Algisite M
510(k) K983210
Algisite M is a Class I device made by Smith & Nephew, Inc., cleared under FDA 510(k) K983210 on 10 Dec 1998, 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 | FDA 510(k)SESE | NumberK983210 | Date10 Dec 1998 | StatusActive |
Official records
- FDA 510(k) database K983210
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KMF
- Device class
- Class I
- Regulation
- 21 CFR Part 880.5090
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent
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