Aequitron Medical, Inc.
Aequitron Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1997.
Top product codes for Aequitron Medical, Inc.
Recent clearances by Aequitron Medical, Inc.
- 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
- K903010 — CONTINUOUS VOLUME VENTILATOR MODEL LP10
- K905244 — MODEL LP6 VENTILATOR, MODIFICATION
- K901656 — MODEL 9200 RESPIRATION/HEART RATE MONITOR
- K902785 — MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
- K901251 — MODEL 9101 RECORDER/ANALYZER SYSTEM
- K882080 — MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.
- K884637 — MODEL 9550/9500 RESPIRATION/HEART RATE MONITOR
- K881266 — MODEL 9216 RESPIRATION/HEART RATE MONITOR
- K872954 — MODEL NUMBER 9216 RESPIRATION/HEART RATE MONITOR
- K871551 — MODEL NUMBER 8200 RESPIRATION/HEART RATE MONITOR
- K853856 — EXTERNAL UTERINE CONTRACTION MONITOR-TOKODYNAMOMET
- K853084 — MEDICON MODEL 8200 AMS(APNEA MONITOR SYSTEM)
- K850181 — AEQUITRON MED-7100 PHOTOTHERAPY LIGHT
- K840358 — IMPEDANCE/8200 MONITOR-MODEL 8300
- K841363 — HEART RATE/RESPIRATION SIMULATOR 8310
- K833348 — RESPIRATION/8100-HEART RATE RECORDER
- K833349 — EVENT TAPE RECORDER 8293
Data sourced from openFDA. This site is unofficial and independent of the FDA.