The following data is part of a premarket notification filed by Closure Medical Corp. with the FDA for Liquiderm Liquid Adhesive Bandage.
| Device ID | K002338 |
| 510k Number | K002338 |
| Device Name: | LIQUIDERM LIQUID ADHESIVE BANDAGE |
| Classification | Bandage, Liquid |
| Applicant | CLOSURE MEDICAL CORP. 5250 GREENS DAIRY RD. Raleigh, NC 27616 |
| Contact | W. Thomas Stephens |
| Correspondent | W. Thomas Stephens CLOSURE MEDICAL CORP. 5250 GREENS DAIRY RD. Raleigh, NC 27616 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-08-01 |
| Decision Date | 2001-01-29 |