The following data is part of a premarket notification filed by Smith & Nephew United, Inc. with the FDA for Cavi-care Conforming Foam Dressing.
Device ID | K943619 |
510k Number | K943619 |
Device Name: | CAVI-CARE CONFORMING FOAM DRESSING |
Classification | Bandage, Liquid |
Applicant | SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
Contact | Jim Irvin |
Correspondent | Jim Irvin SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-27 |
Decision Date | 1994-08-19 |