ULTRA-CORE BIOPSY NEEDLES— 510(k) K921418

Substantially Equivalent

Medical Device Technologies, Inc.

FDA 510(k) clearance K921418 for ULTRA-CORE BIOPSY NEEDLES, Substantially Equivalent on 1992-06-19. Applicant: Medical Device Technologies, Inc..

Clearance details

Applicant: Medical Device Technologies, Inc.
Product code: Code DWO
Advisory panel: General, Plastic Surgery
Date received: 1992-03-24
Decision date: 1992-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gainsville, FL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.