The following data is part of a premarket notification filed by Puritas Health Care, Inc. with the FDA for Multiset.
Device ID | K940055 |
510k Number | K940055 |
Device Name: | MULTISET |
Classification | Set, Blood Transfusion |
Applicant | PURITAS HEALTH CARE, INC. 219 KENT RD. SUITE 20 New Milford, CT 06776 |
Contact | Thomas P Dimaio |
Correspondent | Thomas P Dimaio PURITAS HEALTH CARE, INC. 219 KENT RD. SUITE 20 New Milford, CT 06776 |
Product Code | BRZ |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-01-05 |
Decision Date | 1994-04-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MULTISET 75273625 not registered Dead/Abandoned |
Becton Dickinson and Company 1997-04-14 |
MULTISET 75058999 2045774 Dead/Cancelled |
PCF GROUP, INC. 1996-01-16 |
MULTISET 74559481 1964711 Live/Registered |
SIGNIFY NORTH AMERICA CORPORATION 1994-08-11 |
MULTISET 73773801 1560534 Dead/Cancelled |
BEHNKE, RICHARD R. 1989-01-09 |
MULTISET 73293530 1193081 Dead/Cancelled |
Alphatype Corporation 1981-01-19 |