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FDA 510(k)

ENDOSCOPE ACCESSORY

K-Number: K931895 · 1993-09-07

Decision Date1993-09-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K931895. 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 ENDOSCOPE ACCESSORY?

ENDOSCOPE ACCESSORY is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Applied Medical Resources. The 510(k) number is K931895.

When did ENDOSCOPE ACCESSORY receive FDA 510(k) clearance?

ENDOSCOPE ACCESSORY received FDA 510(k) clearance on 1993-09-07, under 510(k) number K931895.

Who is the listed applicant for ENDOSCOPE ACCESSORY?

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

What is the FDA product code for ENDOSCOPE ACCESSORY?

The FDA product code for ENDOSCOPE ACCESSORY is GCJ.

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 Applied Medical Resources 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 53 devices →

Related Devices (Code: GCJ)

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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