510(k) K880745

LX-100 SLIDE STAINER by Innovative Medical Systems, Inc. — Product Code KPA

K880745 is an FDA 510(k) premarket notification submitted by Innovative Medical Systems, Inc. for the device "LX-100 SLIDE STAINER". The FDA issued a decision of Substantially Equivalent on April 27, 1988. The device falls under product code KPA (Slide Stainer, Automated), a Class I device regulated under 21 CFR 864.3800. Innovative Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 1988
Date Received
February 24, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Slide Stainer, Automated
Device Class
Class I
Regulation Number
864.3800
Review Panel
PA
Submission Type