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FDA 510(k)

IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS

K-Number: K852717 · 1985-07-15

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

Device Summary

IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS 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 K852717. 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 IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS?

IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS 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 K852717.

When did IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS receive FDA 510(k) clearance?

IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS received FDA 510(k) clearance on 1985-07-15, under 510(k) number K852717.

Who is the listed applicant for IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS?

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 IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS?

The FDA product code for IRIS FORCEPS, DELICATE, 1X2 TEETH, STRAIGHT, 4XSS 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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