The following data is part of a premarket notification filed by Hybritech, Inc. with the FDA for Icon Strep B Immunoenzymetric Assay.
Device ID | K902991 |
510k Number | K902991 |
Device Name: | ICON STREP B IMMUNOENZYMETRIC ASSAY |
Classification | Antigens, All Groups, Streptococcus Spp. |
Applicant | HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
Contact | Martinis, Phd |
Correspondent | Martinis, Phd HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
Product Code | GTY |
CFR Regulation Number | 866.3740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-07-09 |
Decision Date | 1990-10-03 |