Product code FES

Device name: Recorder, External, Pressure, Amplifier & Transducer
Medical specialty: Gastroenterology, Urology
Device class: 2
Regulation number: 876.1725
Review panel: GU
Implant: N
Life sustaining/supporting: N
GMP exempt: N
Third party review: Y
Summary malfunction reporting: Eligible
Source: FDA openFDA device classification dataset

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K890284	URODEC 500	Ferguson Medical	1989-05-30
K801757	MMI/GAELTEC CATHETER TIP PRESS. TRANSDU	Medical Measurements, Inc.	1980-08-27