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FDA 510(k)

KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS

K-Number: K852728 · 1985-07-15

ApplicantThe Huxley Instrument Corp.
Decision Date1985-07-15
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS 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 1985-07-15 under 510(k) number K852728. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS?

KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS is a medical device that received FDA 510(k) clearance on 1985-07-15. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852728.

When did KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS receive FDA 510(k) clearance?

KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS received FDA 510(k) clearance on 1985-07-15, under 510(k) number K852728.

Who is the listed applicant for KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS?

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 KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS?

The FDA product code for KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS is HTD.

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Other records listing The Huxley Instrument 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.

K852721BOZEMAN UTERINE FORCEPS, STRAIGHT, 10+410 0R 420K852993BONE RONGEURSK853016STILLE ANGULAR RONGEUR, 8-3/4 SS 410K853015SELF-CENTERING BONE HOLDING FORCEPS, 10-1/4 SS420K852716TAYLOR PERCUSSION HAMMER SS 410 OR 420K852729AALSTEAD MOSQ. FORCEPS, STRAIGHT, 5+SS 410 OR 420

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Related Devices (Code: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.

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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