510(k) K853938

LX 300 TISSUE PROCESSOR by Innovative Medical Systems, Inc. — Product Code IEO

K853938 is an FDA 510(k) premarket notification submitted by Innovative Medical Systems, Inc. for the device "LX 300 TISSUE PROCESSOR". The FDA issued a decision of Substantially Equivalent on October 10, 1985. The device falls under product code IEO (Processor, Tissue, Automated), a Class I device regulated under 21 CFR 864.3875. Innovative Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 10, 1985
Date Received
September 24, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Processor, Tissue, Automated
Device Class
Class I
Regulation Number
864.3875
Review Panel
PA
Submission Type