510(k) K863478

CEREBROSPINAL FLUID PROTEIN TESTPACK, #67668/95 by Em Diagnostic Systems, Inc. — Product Code JGQ

K863478 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "CEREBROSPINAL FLUID PROTEIN TESTPACK, #67668/95". The FDA issued a decision of Substantially Equivalent on October 29, 1986. The device falls under product code JGQ (Turbidimetric, Total Protein), a Class II device regulated under 21 CFR 862.1635. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 29, 1986
Date Received
September 9, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Turbidimetric, Total Protein
Device Class
Class II
Regulation Number
862.1635
Review Panel
CH
Submission Type