REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS— 510(k) K012603
Substantially EquivalentAlliance Medical Corp.
FDA 510(k) clearance K012603 for REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS, Substantially Equivalent on 2001-11-07. Applicant: Alliance Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Alliance Medical Corp.
- Product code
- Code NUJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Phoenix, AZ, US
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More clearances from Alliance Medical Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.