510(k) K913387

DIGITRAPPER MARK III by Synectics-Dantec — Product Code FFT

K913387 is an FDA 510(k) premarket notification submitted by Synectics-Dantec for the device "DIGITRAPPER MARK III". The FDA issued a decision of Substantially Equivalent on December 27, 1991. The device falls under product code FFT (Electrode, Ph, Stomach), a Class I device regulated under 21 CFR 876.1400. Synectics-Dantec has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1991
Date Received
July 29, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Ph, Stomach
Device Class
Class I
Regulation Number
876.1400
Review Panel
GU
Submission Type