SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET— 510(k) K936226

Name: FDA 510(k) clearance K936226
Creator: U.S. Food and Drug Administration
Published: 1994-03-07

Substantially Equivalent

Meadox Medicals, Div. Boston Scientific Corp.

FDA 510(k) clearance K936226 for SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET, Substantially Equivalent on 1994-03-07. Applicant: Meadox Medicals, Div. Boston Scientific Corp.. Device class: 1.

Clearance details

Applicant: Meadox Medicals, Div. Boston Scientific Corp.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1993-12-29
Decision date: 1994-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, NJ, US

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