CORE PREVENT MATTRESS MODIFICATION— 510(k) K935220
Substantially EquivalentPaladin Medical, Inc.
FDA 510(k) clearance K935220 for CORE PREVENT MATTRESS MODIFICATION, Substantially Equivalent on 1993-11-29. Applicant: Paladin Medical, Inc.. Device class: 1.
Clearance details
- Applicant
- Paladin Medical, Inc.
- Product code
- Code FMW
- Device class
- Class 1
- Regulation
- 21 CFR 880.6190
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stillwater, MN, US
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More clearances from Paladin Medical, Inc.
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