BREAST LESION LOCALIZATION NEEDLE— 510(k) K924270

Name: FDA 510(k) clearance K924270
Creator: U.S. Food and Drug Administration
Published: 1992-09-23

Substantially Equivalent

Core Medical, Inc.

FDA 510(k) clearance K924270 for BREAST LESION LOCALIZATION NEEDLE, Substantially Equivalent on 1992-09-23. Applicant: Core Medical, Inc.. Device class: 1.

Clearance details

Applicant: Core Medical, Inc.
Product code: Code GDF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-08-24
Decision date: 1992-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, NC, US

Download summary PDF View on FDA.gov ↗

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