510(k) K872958

IMAGEN INFLUENZA VIRUS A AND B TESTMI by Boots-Celltech Diagnostics, Inc. — Product Code GNX

K872958 is an FDA 510(k) premarket notification submitted by Boots-Celltech Diagnostics, Inc. for the device "IMAGEN INFLUENZA VIRUS A AND B TESTMI". The FDA issued a decision of Substantially Equivalent on February 24, 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. Boots-Celltech Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1988
Date Received
July 29, 1987
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