The following data is part of a premarket notification filed by Unomedical A/s with the FDA for Contact Detach.
| Device ID | K041545 |
| 510k Number | K041545 |
| Device Name: | CONTACT DETACH |
| Classification | Set, Administration, Intravascular |
| Applicant | UNOMEDICAL A/S AAHOLMVEJ 1-3, OSTED Roskilde, DK Dk-4000 |
| Contact | John M Lindskog |
| Correspondent | John M Lindskog UNOMEDICAL A/S AAHOLMVEJ 1-3, OSTED Roskilde, DK Dk-4000 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-09 |
| Decision Date | 2004-06-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00850050080275 | K041545 | 000 |