REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS— 510(k) K012603

Substantially Equivalent

Alliance Medical Corp.

FDA 510(k) clearance K012603 for REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS, Substantially Equivalent on 2001-11-07. Applicant: Alliance Medical Corp..

Clearance details

Applicant: Alliance Medical Corp.
Product code: Code NUJ
Advisory panel: General, Plastic Surgery
Date received: 2001-08-13
Decision date: 2001-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

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