AngioSystems Towel 1002-2
AngioSystems Towel 1002-2 is a surgical drape clip (FDA Class II; FDA product code KKX, Drape, Surgical) made by Angiosystems, Incorporated, cleared under FDA 510(k) K843260 on 21 Sep 1984 and listed in FDA GUDID since 15 Jun 2016 (UDI-DI 00816611020395), active as of 22 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 | Number00816611020395 | Date15 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK843260 | Date21 Sep 1984 | StatusActive |
Official records
- AccessGUDID record 00816611020395
- FDA 510(k) database K843260
Across registries
- FDA 510(k) K843260 decided 21 Sep 1984 Active
- FDA GUDID UDI-DI 00816611020395 listed 15 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K843260
- Listed FDA GUDID 00816611020395
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AngioSystems Towel
- Generic name
- Surgical drape clip, reusable
- Model / reference
- 1002-2
- Primary DI / UDI-DI
- 00816611020395
- 510(k) Number
- FDA product code
- KKX
- GMDN term
- Surgical drape clip, reusable
- Device class
- Class II
- Regulation number
- 878.4370
- GUDID distribution status
- In Commercial Distribution
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- VARIOUS UTILITY/SURGICAL DRAPE, STERILE, DISPOSABL by Trinity Laboratories, Inc.