MODIFIED AIR FLUIDIZED BED, KINAIR— 510(k) K880340
Substantially EquivalentKinetic Concepts, Inc.
FDA 510(k) clearance K880340 for MODIFIED AIR FLUIDIZED BED, KINAIR, Substantially Equivalent on 1988-02-16. Applicant: Kinetic Concepts, Inc.. Device class: 2.
Clearance details
- Applicant
- Kinetic Concepts, Inc.
- Product code
- Code INX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5160
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Antonio, TX, US
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