Precept® 15150
by Precept Medical Products, Inc.
Precept® 15150 is a Class II device made by Precept Medical Products, Inc., cleared under FDA 510(k) K770463 on 23 Mar 1977 and listed in FDA GUDID since 5 Aug 2016 (UDI-DI 10814707020073), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10814707020073 | Date5 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK770463 | Date23 Mar 1977 | StatusActive |
Official records
- AccessGUDID record 10814707020073
- FDA 510(k) database K770463
Across registries
- FDA 510(k) K770463 decided 23 Mar 1977 Active
- FDA GUDID UDI-DI 10814707020073 listed 5 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K770463
- Listed FDA GUDID 10814707020073
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Precept®
- Generic name
- Surgical/medical face mask, single-use
- Model / reference
- 15150
- Primary DI / UDI-DI
- 10814707020073
- 510(k) Number
- FDA product code
- FXX
- GMDN term
- Surgical/medical face mask, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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