The following data is part of a premarket notification filed by Hematology Marketing Assoc. with the FDA for Osmocel 3.
Device ID | K851843 |
510k Number | K851843 |
Device Name: | OSMOCEL 3 |
Classification | Diluent, Blood Cell |
Applicant | HEMATOLOGY MARKETING ASSOC. P.O. BOX 6756 Concord, CA 94524 |
Contact | James Lapicola |
Correspondent | James Lapicola HEMATOLOGY MARKETING ASSOC. P.O. BOX 6756 Concord, CA 94524 |
Product Code | GIF |
CFR Regulation Number | 864.8200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-26 |
Decision Date | 1985-07-30 |