The following data is part of a premarket notification filed by Haemonetics Corp. with the FDA for Fluid Management System (modified).
Device ID | K860969 |
510k Number | K860969 |
Device Name: | FLUID MANAGEMENT SYSTEM (MODIFIED) |
Classification | Pump, Infusion |
Applicant | HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
Contact | Paul H Patrone |
Correspondent | Paul H Patrone HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-03-11 |
Decision Date | 1986-05-06 |