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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Oxford Medilog, Inc. · Predicate Candidate Screening

48 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

84 daysmedian FDA review time
209 days90th percentile
48clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K923737MODEL MEDILOG RAPIDEOxford Medilog, Inc.1994-01-055270
K920295MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)Oxford Medilog, Inc.1992-08-182090
K912890MODEL SONICAID AXISOxford Medilog, Inc.1992-01-091920
K912639SONICAID TEAMOxford Medilog, Inc.1991-12-312000
K904763MENTOR EEG SYSTEMOxford Medilog, Inc.1991-04-101700
K902690SONICAID MODEL MERIDIAN 800Oxford Medilog, Inc.1991-02-052310
K895909SONICAID MODEL VASOFLO 4Oxford Medilog, Inc.1990-07-092720
K896535MEDILOG OPTIMAOxford Medilog, Inc.1990-01-18650
K891383MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEMOxford Medilog, Inc.1989-06-01840
K890330MEDILOG 6000-FD REPORT GENERATOROxford Medilog, Inc.1989-04-20870
K890338MEDILOG EDITOROxford Medilog, Inc.1989-04-19860
K890647MEDILOG 9000-II AMBULATORY RECORDEROxford Medilog, Inc.1989-03-15330
K874917PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEMOxford Medilog, Inc.1988-05-101590
K873680MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEMOxford Medilog, Inc.1987-11-23700
K871990MODEL MPA MULTI PARAMETER ANALYSIS MONITORING SYS.Oxford Medilog, Inc.1987-10-071340
K872497MODEL MR-45 AMBULATORY HOLTER MONITOROxford Medilog, Inc.1987-10-061040
K871500MODEL 5000 AMBULATORY MONITORING SYSTEMOxford Medilog, Inc.1987-07-01760
K863724MODEL 6000 AMBULATORY ECG ANALYSIS SYSTEMOxford Medilog, Inc.1986-11-20580
K862536MODEL 1010 AMBULATORY PH MONITORING SYSTEMOxford Medilog, Inc.1986-09-12720
K860458ELECTROPHYSIOLOGICAL SYSTEM TO MONITOR SKIN TEMP.Oxford Medilog, Inc.1986-08-121880
K860456MODEL 9000 RECORDING & ELECTROPHYSIOLOGICAL SYSTEMOxford Medilog, Inc.1986-08-111870
K860457ELECTROCARDIOGRAPH CONTINUOUS MONITOROxford Medilog, Inc.1986-04-30840
K860455MODEL 9000 RECORDING SYSTEM/RESPIRATION MONITORINGOxford Medilog, Inc.1986-04-01550
K853178SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEMOxford Medilog, Inc.1986-02-282130
K860078MEDILOG 2500 SYSTEMOxford Medilog, Inc.1986-02-26490
K860182MODEL MR-35 HOLTER RECORDEROxford Medilog, Inc.1986-02-26360
K860079MEDILOG 4500 SYSTEMOxford Medilog, Inc.1986-02-26490
K860181MODEL MR-30 HOLTER RECORDEROxford Medilog, Inc.1986-02-26360
K852892MEDILOG M6Oxford Medilog, Inc.1985-12-091530
K850541SLEEP STAGEROxford Medilog, Inc.1985-08-021720
K852883MEDILOG M3Oxford Medilog, Inc.1985-07-26170
K852884MEDILOG M1Oxford Medilog, Inc.1985-07-26170
K850418BUSHEL OFF-HEAD PREAMPLIFIEROxford Medilog, Inc.1985-06-131290
K852207OXFORD VDT-40 DISPLAY TERMINALOxford Medilog, Inc.1985-06-11210
K844736ISISOxford Medilog, Inc.1985-03-211060
K840934MEDILOG PH1Oxford Medilog, Inc.1984-06-281150
K833162AMBULATORY MONITORING DEVICEOxford Medilog, Inc.1984-01-101160
K830915OMAROxford Medilog, Inc.1983-07-071070
K830295MEDILOG 9000 SYSTEMOxford Medilog, Inc.1983-03-24560
K822903AUTOECHOOxford Medilog, Inc.1982-11-01340
K811172VICONOxford Medilog, Inc.1981-06-16490
K802033OXFORD INTENSIVE CARE PATIENT MON. SYSOxford Medilog, Inc.1980-09-26350
K790287ANALYZER, MEDILOG IIOxford Medilog, Inc.1979-02-28200
K790286RECORDER, MEDILOG IIOxford Medilog, Inc.1979-02-27190
K790288STORAGE, DIGITAL DSC-1, CONTROL UNITOxford Medilog, Inc.1979-02-27190
K790289PB-4 REPLAY UNITOxford Medilog, Inc.1979-02-27190
K781129ACCESSORY TO 4-24 RECORDEROxford Medilog, Inc.1978-08-31570
K781130ACCESSORY TO ECG ANALYSIS SYS.Oxford Medilog, Inc.1978-08-23490

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda