KINETIC MOTION BED— 510(k) K823095
Substantially EquivalentMotion Manufacturers, Inc.
FDA 510(k) clearance K823095 for KINETIC MOTION BED, Substantially Equivalent on 1982-12-03. Applicant: Motion Manufacturers, Inc.. Device class: 2.
Clearance details
- Applicant
- Motion Manufacturers, 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
- Mchenry, IL, US
Recent devices under product code IKZ
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