510(k) K850157

CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS by Shaban Mfg. Co. — Product Code KPA

K850157 is an FDA 510(k) premarket notification submitted by Shaban Mfg. Co. for the device "CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS". The FDA issued a decision of Substantially Equivalent on February 27, 1985. The device falls under product code KPA (Slide Stainer, Automated), a Class I device regulated under 21 CFR 864.3800. Shaban Mfg. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 27, 1985
Date Received
January 15, 1985
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