CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1)— 510(k) K963899
Substantially EquivalentExmoor Plastics , Ltd.
FDA 510(k) clearance K963899 for CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1), Substantially Equivalent on 1997-08-22. Applicant: Exmoor Plastics , Ltd.. Device class: 2.
Clearance details
- Applicant
- Exmoor Plastics , Ltd.
- Product code
- Code ETA
- Device class
- Class 2
- Regulation
- 21 CFR 874.3495
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taunton, GB
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More clearances from Exmoor Plastics , Ltd.
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