Atlas FDA

BRAVO PH MONITORING SYSTEM

FDA 510(k) clearance K002028 · decided 2000-09-29

Clearance details

K-number
K002028
Device name
BRAVO PH MONITORING SYSTEM
Applicant
Endonetics, Inc.
Decision
Substantially Equivalent
Date received
2000-07-03
Decision date
2000-09-29
Days to decision
88 days
Clearance type
Traditional
Product code
FFT
Device class
1
Regulation number
876.1400
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Los Gatos, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
BRAVO PH MONITORING SYSTEM AND ACCESSORIES (K102543)Given Imaging , Ltd.2010-12-01
SANDHILL SCIENTIFIC PEDIATEC PH PROBE (K013951)Sandhill Scientific, Inc.2002-02-28
PH ANALYSIS MODULE (K961346)Synectics-Dantec1997-01-29
LOT 440 (K950087)Medical Instruments Corporation Mic AG1996-02-06
TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR (K955018)Instrumentarium Corp.1996-01-30
FLEXILOG 2000 (K945069)Oakfield Instruments, Ltd.1995-06-13
TRIP CIC CATHETER (K920849)Tonometrics, Inc.1995-03-17
CYBERRX MODEL 7200 (K934434)Cybermed Control Systems, Inc.1995-01-24
ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF. (K925405)Synectics-Dantec1994-09-30
SANDHILL DISPOSABLE INTERNAL REFERENCE PH PROBE (K931963)Sandhill Scientific, Inc.1994-09-28
MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATION (K913817)Synectics-Dantec1992-06-11
PH METER, MODIFICATION (K914624)Synectics-Dantec1992-04-28

Recalls involving this device

RecordFirmDate
Given Imaging Bravo pH capsule delivery device, 5-pack. In-Vitro Diagnostic for pH monitor recall (Z-1619-2016)Covidien LLC2016-05-06
Given Imaging Bravo pH capsule delivery device, 1-pack. In- Vitor Diagnostic for pH monito recall (Z-1620-2016)Covidien LLC2016-05-06
Medtronic Bravo pH Capsule with Delivery System, Stomach pH electrode, Product Numbers 901 recall (Z-0517-2008)Medtronic Neuromodulation2008-05-07
Bravo pH Monitoring System Receiver recall (Z-0633-04)Medtronic Gastroenterology / Urology2004-07-20