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FDA 510(k)

ENDOSCOPIC TRAY

K-Number: K771049 · 1977-09-12

ApplicantAmerican Hospital Supply Corp.
Decision Date1977-09-12
Product CodeMMO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1977-09-12 under 510(k) number K771049. The device is classified under product code MMO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC TRAY?

ENDOSCOPIC TRAY is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K771049.

When did ENDOSCOPIC TRAY receive FDA 510(k) clearance?

ENDOSCOPIC TRAY received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771049.

Who is the listed applicant for ENDOSCOPIC TRAY?

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

What is the FDA product code for ENDOSCOPIC TRAY?

The FDA product code for ENDOSCOPIC TRAY is MMO.

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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Other records listing American Hospital Supply 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.

K854739AMERICAN STERILE SURGICAL ABSORBENT TOWELK854759AMERICAN STERILE MAYO STAND TRAYK832826AAP DOSIMETRY RELEASE OR BASIN SETSK830546DOSIMETRIC RELEASEK822990CONVERTORS PRIMARY WOUND DRESSING IIK830343CONTAINER W/PRIMING SOLUTION

View all 56 devices →

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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