510(k) K834599

AUTOTECHNICON V TISSUE PROCESS SYS by Technicon Instruments Corp. — Product Code IEO

K834599 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "AUTOTECHNICON V TISSUE PROCESS SYS". The FDA issued a decision of Substantially Equivalent on February 4, 1984. The device falls under product code IEO (Processor, Tissue, Automated), a Class I device regulated under 21 CFR 864.3875. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1984
Date Received
December 30, 1983
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