SYNTHEMED DEVICE— 510(k) K082276
Substantially EquivalentSynthemed, Inc.
FDA 510(k) clearance K082276 for SYNTHEMED DEVICE, Substantially Equivalent on 2008-11-18. Applicant: Synthemed, Inc.. Device class: 1.
Clearance details
- Applicant
- Synthemed, Inc.
- Product code
- Code LYA
- Device class
- Class 1
- Regulation
- 21 CFR 874.4780
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Recent devices under product code LYA
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