Atlas FDA

QUICKVUE INFLUENZA A+B

FDA 510(k) clearance K131619 · decided 2013-06-28

Clearance details

K-number
K131619
Device name
QUICKVUE INFLUENZA A+B
Applicant
Quidel Corp.
Decision
Substantially Equivalent
Date received
2013-06-03
Decision date
2013-06-28
Days to decision
25 days
Clearance type
Special
Product code
GNX
Device class
1
Regulation number
866.3330
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
San Diego, CA, US
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
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
IMAGEN INFLUENZA VIRUS A AND B TESTMI (K872958)Boots-Celltech Diagnostics, Inc.1988-02-24

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
QUS-2 CALCANEAL ULTRASONOMETER (P990039/S001)Quidel Corp.2003-06-19
QUS-2 (TM) CALCANEAL ULTRASONOMETER (P990039)Quidel Corp.2000-08-01