510(k) K013951

SANDHILL SCIENTIFIC PEDIATEC PH PROBE by Sandhill Scientific, Inc. — Product Code FFT

K013951 is an FDA 510(k) premarket notification submitted by Sandhill Scientific, Inc. for the device "SANDHILL SCIENTIFIC PEDIATEC PH PROBE". The FDA issued a decision of Substantially Equivalent on February 28, 2002. The device falls under product code FFT (Electrode, Ph, Stomach), a Class I device regulated under 21 CFR 876.1400. Sandhill Scientific, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 28, 2002
Date Received
November 30, 2001
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