510(k) K961423

OSOM STREP A TEST by Wyntek Diagnostics, Inc. — Product Code GTZ

K961423 is an FDA 510(k) premarket notification submitted by Wyntek Diagnostics, Inc. for the device "OSOM STREP A TEST". The FDA issued a decision of Substantially Equivalent on October 11, 1996. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Wyntek Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 11, 1996
Date Received
April 12, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, All Groups, Streptococcus Spp.
Device Class
Class I
Regulation Number
866.3740
Review Panel
MI
Submission Type