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 |