PORT-LOCK
Set, Administration, Intravascular
NORFOLK MEDICAL PRODUCTS, INC.
The following data is part of a premarket notification filed by Norfolk Medical Products, Inc. with the FDA for Port-lock.
Pre-market Notification Details
| Device ID | K823845 |
| 510k Number | K823845 |
| Device Name: | PORT-LOCK |
| Classification | Set, Administration, Intravascular |
| Applicant | NORFOLK MEDICAL PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-21 |
| Decision Date | 1983-03-01 |
Trademark Results [PORT-LOCK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PORT-LOCK 73388222 1295893 Dead/Cancelled |
Norfolk Medical Products, Inc. 1982-09-23 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.