FDA 510(k)

ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420

K-Number: K852726 · 1985-07-09

Decision Date1985-07-09

Product CodeKOA

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420 is the device name listed in this FDA 510(k) record. The listed applicant is The Huxley Instrument Corp.. It received FDA 510(k) clearance on 1985-07-09 under 510(k) number K852726. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420?

ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420 is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852726.

When did ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420 receive FDA 510(k) clearance?

ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420 received FDA 510(k) clearance on 1985-07-09, under 510(k) number K852726.

Who is the listed applicant for ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420?

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

What is the FDA product code for ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420?

The FDA product code for ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420 is KOA.

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Other records listing The Huxley Instrument Corp. as applicant

K852721BOZEMAN UTERINE FORCEPS, STRAIGHT, 10+410 0R 420 K852993BONE RONGEURS K853016STILLE ANGULAR RONGEUR, 8-3/4 SS 410 K853015SELF-CENTERING BONE HOLDING FORCEPS, 10-1/4 SS420 K852716TAYLOR PERCUSSION HAMMER SS 410 OR 420 K852728KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS

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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.