510(k) K940026

POLIOVIRUS BLEND MONOCLONAL ANTIBODIES by Light Diagnostics — Product Code GOE

K940026 is an FDA 510(k) premarket notification submitted by Light Diagnostics for the device "POLIOVIRUS BLEND MONOCLONAL ANTIBODIES". The FDA issued a decision of Substantially Equivalent on September 12, 1995. The device falls under product code GOE (Antisera, Fluorescent, Poliovirus 1-3), a Class I device regulated under 21 CFR 866.3405. Light Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 12, 1995
Date Received
January 3, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, Fluorescent, Poliovirus 1-3
Device Class
Class I
Regulation Number
866.3405
Review Panel
MI
Submission Type