The following data is part of a premarket notification filed by Haemonetics Corp. with the FDA for Cell Saver Haemolite B Auto. Blood Recovery System.
| Device ID | K883934 |
| 510k Number | K883934 |
| Device Name: | CELL SAVER HAEMOLITE B AUTO. BLOOD RECOVERY SYSTEM |
| Classification | Apparatus, Autotransfusion |
| Applicant | HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
| Contact | Michael Mathews |
| Correspondent | Michael Mathews HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
| Product Code | CAC |
| CFR Regulation Number | 868.5830 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-15 |
| Decision Date | 1988-12-27 |