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FDA 510(k)

GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS.

K-Number: K851110 · 1985-04-08

ApplicantThe Huxley Instrument Corp.
Decision Date1985-04-08
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. 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 1985-04-08 under 510(k) number K851110. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS.?

GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. is a medical device that received FDA 510(k) clearance on 1985-04-08. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K851110.

When did GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. receive FDA 510(k) clearance?

GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. received FDA 510(k) clearance on 1985-04-08, under 510(k) number K851110.

Who is the listed applicant for GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS.?

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 GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS.?

The FDA product code for GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. is HFB.

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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: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische InstrumenteK930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.

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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