The following data is part of a premarket notification filed by Arrow Intl., Inc. with the FDA for Brachial Plexus Catheter - Bp-01200.
| Device ID | K874105 |
| 510k Number | K874105 |
| Device Name: | BRACHIAL PLEXUS CATHETER - BP-01200 |
| Classification | Anesthesia Conduction Kit |
| Applicant | ARROW INTL., INC. P.O. BOX 6306 HILL AND GEORGE AVENUES Reading, PA 19610 |
| Contact | Thomas D Nickel |
| Correspondent | Thomas D Nickel ARROW INTL., INC. P.O. BOX 6306 HILL AND GEORGE AVENUES Reading, PA 19610 |
| Product Code | CAZ |
| CFR Regulation Number | 868.5140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-09 |
| Decision Date | 1987-11-24 |