510(k) K874459

LIQUI-SERA SPINAL FLUID CONTROL by Biodiagnostic Intl — Product Code JJY

K874459 is an FDA 510(k) premarket notification submitted by Biodiagnostic Intl for the device "LIQUI-SERA SPINAL FLUID CONTROL". The FDA issued a decision of Substantially Equivalent on December 29, 1987. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Biodiagnostic Intl has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 29, 1987
Date Received
October 29, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Multi-Analyte Controls, All Kinds (Assayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type