MAMMARY SIZER— 510(k) K961356

Name: FDA 510(k) clearance K961356
Creator: U.S. Food and Drug Administration
Published: 1996-09-23

Substantially Equivalent for Some Indications

General Surgical Innovations

FDA 510(k) clearance K961356 for MAMMARY SIZER, Substantially Equivalent for Some Indications on 1996-09-23. Applicant: General Surgical Innovations. Device class: Unclassified.

Clearance details

Applicant: General Surgical Innovations
Product code: Code MRD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-04-08
Decision date: 1996-09-23
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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