510(k) K760033

TEST, ANTIBODIES FOR GRP A, LATEX SLIDE by Gamma Biologicals, Inc. — Product Code GTZ

K760033 is an FDA 510(k) premarket notification submitted by Gamma Biologicals, Inc. for the device "TEST, ANTIBODIES FOR GRP A, LATEX SLIDE". The FDA issued a decision of Substantially Equivalent on August 3, 1976. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Gamma Biologicals, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1976
Date Received
June 14, 1976
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