Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE

K-Number: K965154 · 1997-09-19

Decision Date1997-09-19
Product CodeLRT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE is the device name listed in this FDA 510(k) record. The listed applicant is Albert Browne , Ltd.. It received FDA 510(k) clearance on 1997-09-19 under 510(k) number K965154. The device is classified under product code LRT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE?

TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE is a medical device that received FDA 510(k) clearance on 1997-09-19. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K965154.

When did TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE receive FDA 510(k) clearance?

TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE received FDA 510(k) clearance on 1997-09-19, under 510(k) number K965154.

Who is the listed applicant for TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE?

The FDA 510(k) record lists Albert Browne , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE?

The FDA product code for TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE is LRT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Albert Browne , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 19 devices →

Related Devices (Code: LRT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑