510(k) K862536

MODEL 1010 AMBULATORY PH MONITORING SYSTEM by Oxford Medilog, Inc. — Product Code FFT

K862536 is an FDA 510(k) premarket notification submitted by Oxford Medilog, Inc. for the device "MODEL 1010 AMBULATORY PH MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on September 12, 1986. The device falls under product code FFT (Electrode, Ph, Stomach), a Class I device regulated under 21 CFR 876.1400. Oxford Medilog, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 12, 1986
Date Received
July 2, 1986
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