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FDA 510(k)

ENDOSCOPIC BLUNT DISSECTING INSTRUMENT

K-Number: K931854 · 1993-08-10

Decision Date1993-08-10
Product CodeFGS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC BLUNT DISSECTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Mayaguez Medical Center. It received FDA 510(k) clearance on 1993-08-10 under 510(k) number K931854. The device is classified under product code FGS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC BLUNT DISSECTING INSTRUMENT?

ENDOSCOPIC BLUNT DISSECTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1993-08-10. The listed applicant is Mayaguez Medical Center. The 510(k) number is K931854.

When did ENDOSCOPIC BLUNT DISSECTING INSTRUMENT receive FDA 510(k) clearance?

ENDOSCOPIC BLUNT DISSECTING INSTRUMENT received FDA 510(k) clearance on 1993-08-10, under 510(k) number K931854.

Who is the listed applicant for ENDOSCOPIC BLUNT DISSECTING INSTRUMENT?

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

What is the FDA product code for ENDOSCOPIC BLUNT DISSECTING INSTRUMENT?

The FDA product code for ENDOSCOPIC BLUNT DISSECTING INSTRUMENT is FGS.

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 Mayaguez Medical Center 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 10 devices →

Related Devices (Code: FGS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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