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FDA 510(k)

BREVET CASSETTE STERILIZATION MODULE

K-Number: K882617 · 1988-07-28

ApplicantBrevet, Inc.
Decision Date1988-07-28
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BREVET CASSETTE STERILIZATION MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Brevet, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882617. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BREVET CASSETTE STERILIZATION MODULE?

BREVET CASSETTE STERILIZATION MODULE is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Brevet, Inc.. The 510(k) number is K882617.

When did BREVET CASSETTE STERILIZATION MODULE receive FDA 510(k) clearance?

BREVET CASSETTE STERILIZATION MODULE received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882617.

Who is the listed applicant for BREVET CASSETTE STERILIZATION MODULE?

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

What is the FDA product code for BREVET CASSETTE STERILIZATION MODULE?

The FDA product code for BREVET CASSETTE STERILIZATION MODULE is FSM.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Brevet, Inc. 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.

K910794SMALL INSTRUMENT STERILIZATION/BUR BOXK895958BREVET FLOSS PICK (AUTOCLAVE STERILIZER)K895959BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)K895753BREVET DISPOSABLE CONNECTORSK883126BREVET DENTAL INSTRUMENTS

Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.

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.

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