The following data is part of a premarket notification filed by Deknatel, Inc. with the FDA for Pleur-evac--a-5002 Chest Drainage System W/auto.
| Device ID | K880162 |
| 510k Number | K880162 |
| Device Name: | PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO |
| Classification | Apparatus, Autotransfusion |
| Applicant | DEKNATEL, INC. 2300 MARCUS AVE. Lake Success, NY 11042 |
| Contact | Richard J Larkin |
| Correspondent | Richard J Larkin DEKNATEL, INC. 2300 MARCUS AVE. Lake Success, NY 11042 |
| Product Code | CAC |
| CFR Regulation Number | 868.5830 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-01-13 |
| Decision Date | 1988-03-21 |