Skin Support Prep Pad
510(k) K923351
Skin Support Prep Pad is a Class I device made by Coloplast Corp., cleared under FDA 510(k) K923351 on 14 Sep 1992, 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 | NumberK923351 | Date14 Sep 1992 | StatusActive |
Official records
- FDA 510(k) database K923351
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KOX
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4730
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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