KUDO (POWERED ROTATION BED)— 510(k) K905390
Substantially EquivalentKinetic Concepts, Inc.
FDA 510(k) clearance K905390 for KUDO (POWERED ROTATION BED), Substantially Equivalent on 1991-01-08. Applicant: Kinetic Concepts, Inc.. Device class: 2.
Clearance details
- Applicant
- Kinetic Concepts, Inc.
- Product code
- Code IKZ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5225
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Antonio, TX, US
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