510(k) K880460

TARGET STREP A by V-Tech, Inc. — Product Code GTZ

K880460 is an FDA 510(k) premarket notification submitted by V-Tech, Inc. for the device "TARGET STREP A". The FDA issued a decision of Substantially Equivalent on March 3, 1988. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. V-Tech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 3, 1988
Date Received
February 3, 1988
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