The following data is part of a premarket notification filed by Haemonetics Corp. with the FDA for Haemonetics Ln 200f Collection Reservoir.
| Device ID | K904474 |
| 510k Number | K904474 |
| Device Name: | HAEMONETICS LN 200F COLLECTION RESERVOIR |
| Classification | Apparatus, Autotransfusion |
| Applicant | HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
| Contact | Michael P Mathews |
| Correspondent | Michael P 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 | 1990-10-01 |
| Decision Date | 1990-11-13 |