The following data is part of a premarket notification filed by Usci, Div. C.r. Bard, Inc. with the FDA for Catheter, Cardiovascular.
| Device ID | K771823 |
| 510k Number | K771823 |
| Device Name: | CATHETER, CARDIOVASCULAR |
| Classification | Catheter, Flow Directed |
| Applicant | USCI, DIV. C.R. BARD, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DYG |
| CFR Regulation Number | 870.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-09-23 |
| Decision Date | 1977-12-20 |