510(k) K831278

LIQUI-SERA ANTICONVULSANTS CONTROLS by Biodiagnostic Intl — Product Code DIF

K831278 is an FDA 510(k) premarket notification submitted by Biodiagnostic Intl for the device "LIQUI-SERA ANTICONVULSANTS CONTROLS". The FDA issued a decision of Substantially Equivalent on May 27, 1983. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. Biodiagnostic Intl has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1983
Date Received
April 19, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drug Mixture Control Materials
Device Class
Class I
Regulation Number
862.3280
Review Panel
TX
Submission Type