TASSI MK3 (TURNAIR)
FDA 510(k) clearance K910851 · decided 1991-05-15
Clearance details
- K-number
- K910851
- Device name
- TASSI MK3 (TURNAIR)
- Applicant
- Therapy Air Support Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-02-28
- Decision date
- 1991-05-15
- Days to decision
- 76 days
- Clearance type
- Traditional
- Product code
- IOQ
- Device class
- 2
- Regulation number
- 890.5170
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Santa Ana, CA, US
- Third-party review
- No
- Expedited review
- No
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| TOTAL CONTACT SEAT RIPPLE SYSTEM (K943433) | Numotech, Inc. | 1995-07-31 |
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| CLENSICAIR LOW AIRLOSS HYDROTHERAPY (K941610) | Support Systems Intl. | 1995-02-10 |
Recalls involving this device
No recalls on record reference this clearance.