510(k) K914624

PH METER, MODIFICATION by Synectics-Dantec — Product Code FFT

K914624 is an FDA 510(k) premarket notification submitted by Synectics-Dantec for the device "PH METER, MODIFICATION". The FDA issued a decision of Substantially Equivalent on April 28, 1992. 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
April 28, 1992
Date Received
October 16, 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