GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS.— 510(k) K851110

Name: FDA 510(k) clearance K851110
Creator: U.S. Food and Drug Administration
Published: 1985-04-08

Substantially Equivalent

The Huxley Instrument Corp.

FDA 510(k) clearance K851110 for GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS., Substantially Equivalent on 1985-04-08. Applicant: The Huxley Instrument Corp.. Device class: 1.

Clearance details

Applicant: The Huxley Instrument Corp.
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1985-03-19
Decision date: 1985-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Penn Yan, NY, US

Download summary PDF View on FDA.gov ↗

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