Atlas FDA

IMAGEN INFLUENZA VIRUS A AND B TESTMI

FDA 510(k) clearance K872958 · decided 1988-02-24

Clearance details

K-number
K872958
Device name
IMAGEN INFLUENZA VIRUS A AND B TESTMI
Applicant
Boots-Celltech Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1987-07-29
Decision date
1988-02-24
Days to decision
210 days
Clearance type
Traditional
Product code
GNX
Device class
1
Regulation number
866.3330
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Berkshire, England, GB
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ALERE BINAXNOW INFLUENZA A & B CARD (K133411)Alere Scarborough, Inc D/B/A Binax, Inc.2013-12-05
SAS FLUALERT A & B, SAS INFLUENZA A TEST (K132352)Sa Scientific , Ltd.2013-08-22
REMEL XPECT FLU A&B (K131804)Remel, Inc.2013-07-12
QUICK VUE INFLUENZA (K131599)Quidel Corporation2013-07-05
SOFIA INFLUENZA A+B FIA (K131606)Quidel Corp.2013-07-05
QUICKVUE INFLUENZA A+B (K131619)Quidel Corp.2013-06-28
OSOM INFLUENZA A&B TEST MODEL 190 (K123182)SEKISUI Diagnostics, LLC2012-11-05
VIRAZYME INFLUENZA ID TEST FOR INFLUENZA TYPES A AND B VIRUSES (K971494)Zymetx, Inc.1997-09-10
BARTEL PRIMA SYSTEM INFLUENZA A ENZYME IMMUNOASSAY (K924006)Baxter Healthcare Corp1992-12-29
FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE B (K901493)Whittaker Bioproducts, Inc.1990-06-27
FITC MURINE MONOCLONAL ANTI-INFLUENZA TYPE A (K893579)Whittaker Bioproducts, Inc.1990-01-16
INFLUENZA A IFA TEST FOR DIRECT ANTIGEN DETECTION (K884191)Baxter Diagnostics, Inc.1988-11-22

Recalls involving this device

No recalls on record reference this clearance.