510(k) K883599

LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) by Innovative Medical Systems, Inc. — Product Code IEO

K883599 is an FDA 510(k) premarket notification submitted by Innovative Medical Systems, Inc. for the device "LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)". The FDA issued a decision of Substantially Equivalent on September 2, 1988. 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
September 2, 1988
Date Received
August 23, 1988
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