510(k) K970862

SPINALSCOPICS by Quantimetrix Corp. — Product Code JJY

K970862 is an FDA 510(k) premarket notification submitted by Quantimetrix Corp. for the device "SPINALSCOPICS". The FDA issued a decision of Substantially Equivalent on April 8, 1997. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Quantimetrix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 1997
Date Received
March 7, 1997
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