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FDA 510(k)

NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410

K-Number: K852531 · 1985-06-28

ApplicantThe Huxley Instrument Corp.
Decision Date1985-06-28
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410 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 1985-06-28 under 510(k) number K852531. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410?

NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410 is a medical device that received FDA 510(k) clearance on 1985-06-28. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852531.

When did NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410 receive FDA 510(k) clearance?

NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410 received FDA 510(k) clearance on 1985-06-28, under 510(k) number K852531.

Who is the listed applicant for NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410?

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 NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410?

The FDA product code for NON-PERFORATING TOWEL FORCEPS-5-1/4 IN SS 410 is GEN.

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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 420K852728KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS

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Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, 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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