14.5-16.0 FRENCH CUFFED CATHETER REMOVAL DEVICE, SYMMETRY SURGICAL SINGEL USE— 510(k) K122263
Substantially EquivalentSymmetry Medical
FDA 510(k) clearance K122263 for 14.5-16.0 FRENCH CUFFED CATHETER REMOVAL DEVICE, SYMMETRY SURGICAL SINGEL USE, Substantially Equivalent on 2012-09-28. Applicant: Symmetry Medical. Device class: 2.
Clearance details
- Applicant
- Symmetry Medical
- Product code
- Code ODY
- Device class
- Class 2
- Regulation
- 21 CFR 880.5970
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Antioch, TN, US
Recent devices under product code ODY
view allMore clearances from Symmetry Medical
view allData sourced from openFDA. This site is unofficial and independent of the FDA.