FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EXTERNAL UTERINE CONTRACTION MONITOR-TOKODYNAMOMET

K Number: K853856 · Decision Mar 12, 1986
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
22
Applicant Total
24
Review Days
177

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EXTERNAL UTERINE CONTRACTION MONITOR-TOKODYNAMOMET
K Number
K853856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Aequitron Medical, Inc.
Date Received
September 16, 1985
Decision Date
March 12, 1986
Product Code
HFM
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HFM Monitor, Uterine Contraction, External (For Use In Clinic)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HFM), ordered by most recent decision date.

View all

Other Clearances by Aequitron Medical, Inc.

K Number Device Name
K961972 MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
K952880 MODEL LP-1000 VOLUME VENTILATOR
K944654 OXYGEN CONCENTRATION INDICATOR
K914424 MODEL 6213 REMOTE ALARM
K915381 PORTABLE OXYGEN GENERATOR
K911399 NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)
K903020 RESPIRATION/HEART RATE MONITOR MODEL 9500/9550
K905244 MODEL LP6 VENTILATOR, MODIFICATION
K903010 CONTINUOUS VOLUME VENTILATOR MODEL LP10
K902785 MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
Search all 24 clearances from Aequitron Medical, Inc. →