Tennessee House Bill HB1452

Tennessee 2023-2024 Regular Session

• Introduced: 1/31/23
• Refer: 2/14/23
• Refer: 2/21/23
• Refer: 2/28/23
• Refer: 4/18/23
• Chaptered: 5/24/23
• Passed: 5/24/23

Caption

AN ACT to amend Tennessee Code Annotated, Title 68, Chapter 122, relative to boilers.

Impact

The proposed amendments aim to streamline the regulatory framework surrounding boilers and pressure vessels in Tennessee, particularly for businesses involved in healthcare equipment. By clarifying definitions and operational guidelines, the bill seeks to improve compliance for manufacturers and users of medical devices, thereby enhancing safety and efficiency in the healthcare sector. However, the omission of specific regulatory requirements for certain types of pressure vessels could lead to concerns regarding safety standards in environments where these devices are employed.

Summary

House Bill 1452 seeks to amend the Tennessee Code Annotated, specifically Title 68, Chapter 122, focusing on the regulation of boilers and unfired pressure vessels. The bill introduces definitions for 'autoclave' and 'miniature boiler,' specifying their dimensions and operational pressures. Additionally, it outlines exemptions regarding the regulation of certain unfired pressure vessels, particularly those used in medical applications. This change is intended to clarify existing laws and ensure consistency in the application of regulations related to these devices.

Sentiment

Overall, the sentiment surrounding HB1452 appears to be practical, focusing on improving regulatory clarity and safety in the medical field. Supporters of the bill argue that it will reduce bureaucratic barriers for healthcare providers and manufacturers, facilitating better medical care. On the other hand, critics may express concerns that the bill could lead to a dilution of safety regulations, particularly if the definitions or operational pressures allow for broader exemptions than currently exist.

Contention

Notable points of contention arise from the implications of reclassifying certain devices and the potential impact on safety oversight. Stakeholders in the healthcare sector may have differing views on how the amendments could affect operational standards and accountability. There is a tension between the desire to promote innovation and efficiency in medical equipment regulation and the need to ensure that safety standards are maintained across all types of pressure vessels.