Salter Labs - FDA 510(k) Cleared Devices
48
Total
48
Cleared
0
Denied
Salter Labs has 48 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 48 cleared submissions from 1978 to 2017.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
48 devices
Cleared
Sep 21, 2017
Salter Labs Bubble Humidifier
Anesthesiology
456d
Cleared
Apr 15, 2016
BiNAPS Nasal Airflow and Snore Transducer
Anesthesiology
281d
Cleared
Mar 11, 2016
Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula
Anesthesiology
281d
Cleared
Mar 10, 2016
Nasal CO2 Sample Line, Oral Nasal CO2 Sampling Cannula, O2 Oral/Nasal Co2...
Anesthesiology
287d
Cleared
Aug 05, 2015
CPAP Cannulaide
Anesthesiology
224d
Cleared
Jun 12, 2015
Luma Wrap
General Hospital
288d
Cleared
Nov 24, 2009
PNEUMOTHERML, MODEL: 5800
Anesthesiology
83d
Cleared
Sep 15, 2005
BI-NAPS NASAL AIRFLOW AND SNORE TRANSDUCER
Anesthesiology
119d
Cleared
Mar 04, 2005
SALTER LABS CPAP HIGH FLOW CANNULA SYSTEM
Anesthesiology
400d
Cleared
Feb 01, 2002
SALTER LABS MODIFIED NEBUTECH NEBULIZER
Anesthesiology
53d
Cleared
Jan 07, 2000
SALTER AIRE COMPRESSOR
Anesthesiology
184d
Cleared
Sep 24, 1999
SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER
Anesthesiology
21d
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