The following data is part of a premarket notification filed by Diagnostic Specialties with the FDA for Enzip Immunoturbidmetric Fibrinogen Assay Kit.
Device ID | K941001 |
510k Number | K941001 |
Device Name: | ENZIP IMMUNOTURBIDMETRIC FIBRINOGEN ASSAY KIT |
Classification | Test, Fibrinogen |
Applicant | DIAGNOSTIC SPECIALTIES 4 LEONARD ST. Metuchen, NJ 08840 -4338 |
Contact | Rinaldo Pagnucco |
Correspondent | Rinaldo Pagnucco DIAGNOSTIC SPECIALTIES 4 LEONARD ST. Metuchen, NJ 08840 -4338 |
Product Code | GIS |
CFR Regulation Number | 864.7340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-03-01 |
Decision Date | 1994-08-30 |