Peanut 40-03
by American Surgical Company, LLC
Peanut 40-03 is a dissection sponge (FDA Class I; FDA product code GDY, Gauze/Sponge, Internal, X-Ray Detectable) made by American Surgical Company, LLC, cleared under FDA 510(k) K872809 on 4 Aug 1987 and listed in FDA GUDID since 30 Jun 2016 (UDI-DI 20749915000692), 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 | Number20749915000692 | Date30 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK872809 | Date4 Aug 1987 | StatusActive |
Official records
- AccessGUDID record 20749915000692
- FDA 510(k) database K872809
Across registries
- FDA 510(k) K872809 decided 4 Aug 1987 Active
- FDA GUDID UDI-DI 20749915000692 listed 30 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K872809
- Listed FDA GUDID 20749915000692
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Peanut
- Generic name
- Dissection sponge
- Model / reference
- 40-03
- Primary DI / UDI-DI
- 20749915000692
- 510(k) Number
- FDA product code
- GDY
- GMDN term
- Dissection sponge
- Device class
- Class I
- Regulation number
- 878.4450
- GUDID distribution status
- In Commercial Distribution
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