SALONMAY BUSTLINE INCREASER
FDA 510(k) clearance K770082 · decided 1977-03-16
Clearance details
- K-number
- K770082
- Device name
- SALONMAY BUSTLINE INCREASER
- Applicant
- Gamma Enterprises, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-01-14
- Decision date
- 1977-03-16
- Days to decision
- 61 days
- Clearance type
- Traditional
- Product code
- MWZ
- Device class
- 1
- Regulation number
- 890.5660
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.