Non-Absorbable Surgical Sutures
510(k) K930517
Non-Absorbable Surgical Sutures is a Class II device made by Alcon Laboratories, Inc., cleared under FDA 510(k) K930517 on 17 Dec 1993, 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 | NumberK930517 | Date17 Dec 1993 | StatusActive |
Official records
- FDA 510(k) database K930517
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GAR
- FDA applicant
- Alcon Laboratories
- Device class
- Class II
- Regulation
- 21 CFR Part 878.5020
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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- DemeLON NL296011F14P by DemeTECH Corp
- NUROLON C512D by Ethicon Inc.
- MANI NEEDLE & SUTURE PACK (NYLON) by MANI, INC.
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- SILK SUTURES-REVISED LABELING by Look, Inc.
- Supramid Extra Sutures by S. Jackson, Inc.