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FDA 510(k)

MICROPROCESSED CONTROLLED LAPAROFLATOR

K-Number: K913242 · 1992-09-25

ApplicantBryan Corp.
Decision Date1992-09-25
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MICROPROCESSED CONTROLLED LAPAROFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Bryan Corp.. It received FDA 510(k) clearance on 1992-09-25 under 510(k) number K913242. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPROCESSED CONTROLLED LAPAROFLATOR?

MICROPROCESSED CONTROLLED LAPAROFLATOR is a medical device that received FDA 510(k) clearance on 1992-09-25. The listed applicant is Bryan Corp.. The 510(k) number is K913242.

When did MICROPROCESSED CONTROLLED LAPAROFLATOR receive FDA 510(k) clearance?

MICROPROCESSED CONTROLLED LAPAROFLATOR received FDA 510(k) clearance on 1992-09-25, under 510(k) number K913242.

Who is the listed applicant for MICROPROCESSED CONTROLLED LAPAROFLATOR?

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

What is the FDA product code for MICROPROCESSED CONTROLLED LAPAROFLATOR?

The FDA product code for MICROPROCESSED CONTROLLED LAPAROFLATOR is HIF.

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.

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Other records listing Bryan Corp. 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.

K002063BIOTRACE, MODEL 1730K894380DUMON TRACHEOBRONCHIAL STENTK881249BAGGISH, HYSTEROSCOPEK854414DUMON/HARRELL

Related Devices (Code: HIF)

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.

K260209ENDOFLATOR+; Smart Smoke EvacuationKarl Storz SE & CO. KGK252584Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)Weyo Surgical Technology , Ltd.K252318Insufflator (OPTO-IFL1000)Guangdong Optomedic Technologies, Inc.K250388ENDOFLATOR +Karl Storz SE & CO. KGK242772AirSurgN Insufflator (10030/AirSurgN)SmartsurgN, Inc.K243527High Flow Insufflation Unit (UHI-4)Olympus Medical Systems Corporation

Official Source

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

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