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FDA 510(k)

INMAN ENDOSCOPIC BLUNT DISSECTOR

K-Number: K933169 · 1994-04-19

ApplicantInman Medical Corp.
Decision Date1994-04-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INMAN ENDOSCOPIC BLUNT DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K933169. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INMAN ENDOSCOPIC BLUNT DISSECTOR?

INMAN ENDOSCOPIC BLUNT DISSECTOR is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Inman Medical Corp.. The 510(k) number is K933169.

When did INMAN ENDOSCOPIC BLUNT DISSECTOR receive FDA 510(k) clearance?

INMAN ENDOSCOPIC BLUNT DISSECTOR received FDA 510(k) clearance on 1994-04-19, under 510(k) number K933169.

Who is the listed applicant for INMAN ENDOSCOPIC BLUNT DISSECTOR?

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

What is the FDA product code for INMAN ENDOSCOPIC BLUNT DISSECTOR?

The FDA product code for INMAN ENDOSCOPIC BLUNT DISSECTOR is GCJ.

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Other records listing Inman Medical 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.

K933171INMAN IRRIGATION TAPERED PROBEK933094INSUFFLATOR TUBING KIT W/FILTERK933382IMC CABLE/WIRE COVERK933774IMC SALINE WET DRESSINGK933305IMC 5.0MM IRRIGATION/ASPIRATION PROBEK933306IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES

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Related Devices (Code: GCJ)

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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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