Critical Cover 608
Critical Cover 608 is a Class II device made by Alphaprotech, Inc., cleared under FDA 510(k) K890128 on 14 Feb 1989 and listed in FDA GUDID since 3 Nov 2016 (UDI-DI 10817583020014), 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 | Number10817583020014 | Date3 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK890128 | Date14 Feb 1989 | StatusActive |
Official records
- AccessGUDID record 10817583020014
- FDA 510(k) database K890128
Across registries
- FDA 510(k) K890128 decided 14 Feb 1989 Active
- FDA GUDID UDI-DI 10817583020014 listed 3 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K890128
- Listed FDA GUDID 10817583020014
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Critical Cover
- Generic name
- Surgical/medical face mask, non-antimicrobial, single-use
- Model / Ref / Catalog
- 608
- Primary DI / UDI-DI
- 10817583020014
- 510(k) Number
- FDA product code
- FXX
- GMDN term
- Surgical/medical face mask, non-antimicrobial, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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