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FDA 510(k)

MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR

K-Number: K915694 · 1992-06-18

ApplicantMedical Devices, Inc.
Decision Date1992-06-18
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1992-06-18 under 510(k) number K915694. 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 MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR?

MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR is a medical device that received FDA 510(k) clearance on 1992-06-18. The listed applicant is Medical Devices, Inc.. The 510(k) number is K915694.

When did MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR receive FDA 510(k) clearance?

MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR received FDA 510(k) clearance on 1992-06-18, under 510(k) number K915694.

Who is the listed applicant for MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR?

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

What is the FDA product code for MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR?

The FDA product code for MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR is HIF.

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Other records listing Medical Devices, Inc. as applicant

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K002280PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602K930084MICRO-ARTHROSCOPEK943126ELECTROFLEXK940012SMARTBRACE ELECTRODEK935132HOME MICROCURRENT HMCK934619FLEXMATE

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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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