The following data is part of a premarket notification filed by E-z-em, Inc. with the FDA for E-z-flow Angiography Catheters.
| Device ID | K890206 |
| 510k Number | K890206 |
| Device Name: | E-Z-FLOW ANGIOGRAPHY CATHETERS |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | E-Z-EM, INC. 28 MARIGOLD LN. Marlboro, NJ 07746 |
| Contact | Martin S Knopf |
| Correspondent | Martin S Knopf E-Z-EM, INC. 28 MARIGOLD LN. Marlboro, NJ 07746 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-17 |
| Decision Date | 1989-05-19 |