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FDA 510(k)

M.I.S. TROCAR-CANNULA

K-Number: K925276 · 1993-05-24

ApplicantM.I.S. Technology, Inc.
Decision Date1993-05-24
Product CodeGCS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

M.I.S. TROCAR-CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is M.I.S. Technology, Inc.. It received FDA 510(k) clearance on 1993-05-24 under 510(k) number K925276. The device is classified under product code GCS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.I.S. TROCAR-CANNULA?

M.I.S. TROCAR-CANNULA is a medical device that received FDA 510(k) clearance on 1993-05-24. The listed applicant is M.I.S. Technology, Inc.. The 510(k) number is K925276.

When did M.I.S. TROCAR-CANNULA receive FDA 510(k) clearance?

M.I.S. TROCAR-CANNULA received FDA 510(k) clearance on 1993-05-24, under 510(k) number K925276.

Who is the listed applicant for M.I.S. TROCAR-CANNULA?

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

What is the FDA product code for M.I.S. TROCAR-CANNULA?

The FDA product code for M.I.S. TROCAR-CANNULA is GCS.

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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Related Devices (Code: GCS)

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.

K944062LAPRASCOPIC GRASPERInstrument Makar, Inc.K944067PEANUT WAND, MODIFICATIONIdeal Medical, Inc.K933201AESCULAP TROCAR INSTRUMENT SETAesculap, Inc.K93276210.0MM SUCTION/IRRIGATION PROBE & TUBING KITInman Medical Corp.K933371IMC ENDOSCOPIC INSTRUMENT HOLDERInman Medical Corp.K924134LEISEGANG LAPAROSCOPIC IRRIGATION SYSTEM/ACCESSLeisegang Medical, 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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