The following data is part of a premarket notification filed by Hemagen Diagnostics, Inc. with the FDA for Virgo Anca Screen Kit.
Device ID | K973822 |
510k Number | K973822 |
Device Name: | VIRGO ANCA SCREEN KIT |
Classification | Test System, Antineutrophil Cytoplasmic Antibodies (anca) |
Applicant | HEMAGEN DIAGNOSTICS, INC. 34-40 BEAR HILL RD. Waltlham, MA 02154 |
Contact | Joseph M Califano |
Correspondent | Joseph M Califano HEMAGEN DIAGNOSTICS, INC. 34-40 BEAR HILL RD. Waltlham, MA 02154 |
Product Code | MOB |
CFR Regulation Number | 866.5660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-10-07 |
Decision Date | 1997-11-13 |
Summary: | summary |