The following data is part of a premarket notification filed by Coloplast Corp. with the FDA for Contreet Foam Adhesive/non-adhesive.
| Device ID | K022416 |
| 510k Number | K022416 |
| Device Name: | CONTREET FOAM ADHESIVE/NON-ADHESIVE |
| Classification | Dressing, Wound, Drug |
| Applicant | COLOPLAST CORP. 1940 COMMERCE DR. North Mankato, MN 56003 |
| Contact | Elizabeth Boots |
| Correspondent | Elizabeth Boots COLOPLAST CORP. 1940 COMMERCE DR. North Mankato, MN 56003 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-24 |
| Decision Date | 2003-02-03 |
| Summary: | summary |