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FDA 510(k)

40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0

K-Number: K022052 · 2003-01-24

ApplicantNorthgate Technologies, Inc.
Decision Date2003-01-24
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0 is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 2003-01-24 under 510(k) number K022052. 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 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0?

40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0 is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K022052.

When did 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0 receive FDA 510(k) clearance?

40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0 received FDA 510(k) clearance on 2003-01-24, under 510(k) number K022052.

Who is the listed applicant for 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0?

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

What is the FDA product code for 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0?

The FDA product code for 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0 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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