The following data is part of a premarket notification filed by Schiapparelli Biosystems, Inc. with the FDA for Ace Phenytoin Reagent, Aed Calibrators.
Device ID | K973414 |
510k Number | K973414 |
Device Name: | ACE PHENYTOIN REAGENT, AED CALIBRATORS |
Classification | Enzyme Immunoassay, Diphenylhydantoin |
Applicant | SCHIAPPARELLI BIOSYSTEMS, INC. 368 PASSAIC AVE. Fairfield, NJ 07004 |
Contact | Steven Dalessio |
Correspondent | Steven Dalessio SCHIAPPARELLI BIOSYSTEMS, INC. 368 PASSAIC AVE. Fairfield, NJ 07004 |
Product Code | DIP |
CFR Regulation Number | 862.3350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-09 |
Decision Date | 1997-11-04 |
Summary: | summary |