Atlas FDA

QUIDEL GROUP B STREP TEST

FDA 510(k) clearance K896265 · decided 1990-02-16

Clearance details

K-number
K896265
Device name
QUIDEL GROUP B STREP TEST
Applicant
Quidel Corp.
Decision
Substantially Equivalent
Date received
1989-10-31
Decision date
1990-02-16
Days to decision
108 days
Clearance type
Traditional
Product code
GTZ
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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Similar devices under this product code

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

RecordFirmDate
BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST (K012521)Binax, Inc.2001-11-30
UNI-GOLD STREP A TEST KIT (K011709)Trinity Biotech, Plc2001-11-08
MODIFICATION TO BINAX NOW STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST (K010523)Binax, Inc.2001-03-15
BINAX NOWR STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST (22 TEST KIT),(12 TEST KIT), BINAX NOWR STREPTOCOCCUS PNEUMONI (K991726)Binax, Inc.1999-08-27
ABBOTT TESTPACK PLUS STREP A WITH ON BOARD CONTROLS (OBC) II (K971522)Abbott Laboratories1998-03-03
STREP A OIA MAX (K962060)Biostar, Inc.1997-07-23
STREPTOLEX-STAT (K962296)Unipath , Ltd.1996-12-16
OSOM STREP A TEST (K961423)Wyntek Diagnostics, Inc.1996-10-11
EXCEL ONESTEP GROUP A STREP ANTIGEN MODULE TEST KIT (K962146)Excel Scientific, Inc.1996-10-07
CARDS Q.S. STREP A (K955108)Quidel Corp.1996-04-15
BINAX STREP A TEST (K960712)Binax, Inc.1996-03-22
ABBOTT TESTPACK PLUS STREP A WITH ON BOARD CONTROLS (OBC) (K952819)Abbott Laboratories1996-01-26

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