510(k) K895281

TRANSDUCER PROTECTOR by Filtertek, Inc. — Product Code FIB

K895281 is an FDA 510(k) premarket notification submitted by Filtertek, Inc. for the device "TRANSDUCER PROTECTOR". The FDA issued a decision of Substantially Equivalent on November 8, 1989. The device falls under product code FIB (Protector, Transducer, Dialysis), a Class II device regulated under 21 CFR 876.5820. Filtertek, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1989
Date Received
August 24, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Protector, Transducer, Dialysis
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type