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FDA 510(k)

IMC ENDOSCOPIC INSTRUMENT HOLDER

K-Number: K933371 · 1993-08-06

Decision Date1993-08-06
Product CodeGCS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IMC ENDOSCOPIC INSTRUMENT HOLDER 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 1993-08-06 under 510(k) number K933371. 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 IMC ENDOSCOPIC INSTRUMENT HOLDER?

IMC ENDOSCOPIC INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Inman Medical Corp.. The 510(k) number is K933371.

When did IMC ENDOSCOPIC INSTRUMENT HOLDER receive FDA 510(k) clearance?

IMC ENDOSCOPIC INSTRUMENT HOLDER received FDA 510(k) clearance on 1993-08-06, under 510(k) number K933371.

Who is the listed applicant for IMC ENDOSCOPIC INSTRUMENT HOLDER?

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 IMC ENDOSCOPIC INSTRUMENT HOLDER?

The FDA product code for IMC ENDOSCOPIC INSTRUMENT HOLDER 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.

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.

View all 14 devices →

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.

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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