FDA 510(k)

SUTURE WOUND TRAY MILFORD WHITTINSVILLE

K-Number: K802386 · 1980-11-12

ApplicantAmerican Medical Disposable, Inc.

Decision Date1980-11-12

Product CodeFMC

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SUTURE WOUND TRAY MILFORD WHITTINSVILLE is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Disposable, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802386. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE WOUND TRAY MILFORD WHITTINSVILLE?

SUTURE WOUND TRAY MILFORD WHITTINSVILLE is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is American Medical Disposable, Inc.. The 510(k) number is K802386.

When did SUTURE WOUND TRAY MILFORD WHITTINSVILLE receive FDA 510(k) clearance?

SUTURE WOUND TRAY MILFORD WHITTINSVILLE received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802386.

Who is the listed applicant for SUTURE WOUND TRAY MILFORD WHITTINSVILLE?

The FDA 510(k) record lists American Medical Disposable, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE WOUND TRAY MILFORD WHITTINSVILLE?

The FDA product code for SUTURE WOUND TRAY MILFORD WHITTINSVILLE is FMC.

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Other records listing American Medical Disposable, Inc. as applicant

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Related Devices (Code: FMC)

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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.