510(k) K834599
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