Atlas FDA

ICON STREP B IMMUNOENZYMETRIC ASSAY

FDA 510(k) clearance K902991 · decided 1990-10-03

Clearance details

K-number
K902991
Device name
ICON STREP B IMMUNOENZYMETRIC ASSAY
Applicant
Hybritech, Inc.
Decision
Substantially Equivalent
Date received
1990-07-09
Decision date
1990-10-03
Days to decision
86 days
Clearance type
Traditional
Product code
GTY
Device class
1
Regulation number
866.3740
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
TANDEM(R) E CEA IMMUNORADIOMETRIC ASSAY (P840019/S012)Hybritech, Inc.1996-03-07
STRATUS (R) CEA FLUOROMETRIC ENZYME IMMUNOASSAY (P840019/S010)Hybritech, Inc.1994-03-17
TANDEM(R) R CEA IMMUNORADIOMETRIC ASSAY (P840019/S011)Hybritech, Inc.1994-01-13
TANDEM-R(R) CARCINOEMBRYONIC ANTIGEN (CEA) ASSAY (P840019/S009)Hybritech, Inc.1990-04-17
TANDEM(R)-R CARCINOEMBRYONIC ANTIGEN ASSAY (P840019/S008)Hybritech, Inc.1989-12-13
TANDEM(R)-R CARCINOEMBRYONIC ANTIGEN ASSAY (P840019/S007)Hybritech, Inc.1989-09-06
TANDEM(R)-R CARCINOEMBRYONIC ANTIGEN ASSAY (P840019/S006)Hybritech, Inc.1987-04-30
TANDEM(R)-R CARCINOEMBRYONIC ANTIGEN ASSAY (P840019/S005)Hybritech, Inc.1986-11-05