510(k) K884191

INFLUENZA A IFA TEST FOR DIRECT ANTIGEN DETECTION by Baxter Diagnostics, Inc. — Product Code GNX

K884191 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "INFLUENZA A IFA TEST FOR DIRECT ANTIGEN DETECTION". The FDA issued a decision of Substantially Equivalent on November 22, 1988. 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. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 22, 1988
Date Received
October 6, 1988
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