510(k) K922081

LABOTECH AUTOMATED MICROTITER ANALYZER by Innovative Medical Systems, Inc. — Product Code JJQ

K922081 is an FDA 510(k) premarket notification submitted by Innovative Medical Systems, Inc. for the device "LABOTECH AUTOMATED MICROTITER ANALYZER". The FDA issued a decision of Substantially Equivalent on September 2, 1992. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Innovative Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 2, 1992
Date Received
May 5, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class
Class I
Regulation Number
862.2300
Review Panel
CH
Submission Type