Intermittent Pressure Pad
by Flowtron-Aire, Ltd. 510(k)
Active
510(k) K761227
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK761227 | Date14 Dec 1976 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 10 Oct 2026.
Specification
- 510(k) Number
- FDA applicant
- Flowtron-Aire , Ltd.
- Advisory Committee
- Unknown
- FDA Decision
- SESE Substantially Equivalent