SURETEK REPROCESSED LAPAROSCOPIC INSTRUMENTS— 510(k) K052690
Substantially EquivalentSuretek Medical
FDA 510(k) clearance K052690 for SURETEK REPROCESSED LAPAROSCOPIC INSTRUMENTS, Substantially Equivalent on 2006-05-12. Applicant: Suretek Medical.
Clearance details
- Applicant
- Suretek Medical
- Product code
- Code NUJ
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Greenville, SC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.