HANDY VIBRO BELT
FDA 510(k) clearance K925036 · decided 1993-06-29
Clearance details
- K-number
- K925036
- Device name
- HANDY VIBRO BELT
- Applicant
- Cosmesearch, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-10-05
- Decision date
- 1993-06-29
- Days to decision
- 267 days
- Clearance type
- Traditional
- Product code
- ISA
- Device class
- 1
- Regulation number
- 890.5660
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Solana Beach, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.