510(k) K912394

TRANSDUCER PROTECTOR by Filtertek, Inc. — Product Code FIB

K912394 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 August 30, 1991. 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
August 30, 1991
Date Received
May 28, 1991
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