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FDA 510(k)

LAPAROSCOPIC INSUFLATION Y TUBING

K-Number: K911479 · 1991-04-29

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-04-29
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC INSUFLATION Y TUBING is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K911479. 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 LAPAROSCOPIC INSUFLATION Y TUBING?

LAPAROSCOPIC INSUFLATION Y TUBING is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911479.

When did LAPAROSCOPIC INSUFLATION Y TUBING receive FDA 510(k) clearance?

LAPAROSCOPIC INSUFLATION Y TUBING received FDA 510(k) clearance on 1991-04-29, under 510(k) number K911479.

Who is the listed applicant for LAPAROSCOPIC INSUFLATION Y TUBING?

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

What is the FDA product code for LAPAROSCOPIC INSUFLATION Y TUBING?

The FDA product code for LAPAROSCOPIC INSUFLATION Y TUBING is HIF.

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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

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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