Cleared Traditional

DETECT-A-STREP

K843590 · Antibodies, Inc. · Microbiology
Oct 1984
Decision
48d
Days
Class 1
Risk

About This 510(k) Submission

K843590 is an FDA 510(k) clearance for the DETECT-A-STREP, a Antisera, All Groups, Streptococcus Spp. (Class I — General Controls, product code GTZ), submitted by Antibodies, Inc. (Davis, US). The FDA issued a Cleared decision on October 30, 1984, 48 days after receiving the submission on September 12, 1984. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.3740.

Submission Details

510(k) Number K843590 FDA.gov
FDA Decision Cleared SESE
Date Received September 12, 1984
Decision Date October 30, 1984
Days to Decision 48 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary —

Device Classification

Product Code GTZ — Antisera, All Groups, Streptococcus Spp.
Device Class Class I — General Controls
CFR Regulation 21 CFR 866.3740

Similar Devices — GTZ Antisera, All Groups, Streptococcus Spp.

All 104
BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST
K012521 · Binax, Inc. · Nov 2001
UNI-GOLD STREP A TEST KIT
K011709 · Trinity Biotech, Plc · Nov 2001
MODIFICATION TO BINAX NOW STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST
K010523 · Binax, Inc. · Mar 2001
BINAX NOWR STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST (22 TEST KIT),(12 TEST KIT), BINAX NOWR STREPTOCOCCUS PNEUMONI
K991726 · Binax, Inc. · Aug 1999
ABBOTT TESTPACK PLUS STREP A WITH ON BOARD CONTROLS (OBC) II
K971522 · Abbott Laboratories · Mar 1998
STREP A OIA MAX
K962060 · Biostar, Inc. · Jul 1997