510(k) K802931

INFLUENZA A & B S-ANTIGEN & CONTROLS by Orion Diagnostica, Inc. — Product Code GNX

K802931 is an FDA 510(k) premarket notification submitted by Orion Diagnostica, Inc. for the device "INFLUENZA A & B S-ANTIGEN & CONTROLS". The FDA issued a decision of Substantially Equivalent on January 12, 1981. The device falls under product code GNX (Antigens, Cf (Including Cf Control), Influenza Virus A, B, C), a Class I device regulated under 21 CFR 866.3330. Orion Diagnostica, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 12, 1981
Date Received
November 19, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigens, Cf (Including Cf Control), Influenza Virus A, B, C
Device Class
Class I
Regulation Number
866.3330
Review Panel
MI
Submission Type