SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS— 510(k) K930773

Name: FDA 510(k) clearance K930773
Creator: U.S. Food and Drug Administration
Published: 1994-07-28

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K930773 for SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS, Substantially Equivalent on 1994-07-28. Applicant: Symbiosis Corp.. Device class: 1.

Clearance details

Applicant: Symbiosis Corp.
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1993-02-16
Decision date: 1994-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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