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Sdi Diagnostics, Inc.

10 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
IQSense Flow Sensor Mouthpiece (K150515)Sdi Diagnostics, Inc.2016-01-12
ASTRASONIC SPIROMETER, MODEL 29-8000 (K092813)Sdi Diagnostics, Inc.2010-07-16
ASTRA 300 (K061571)Sdi Diagnostics, Inc.2007-01-31
ASTRAGUARD PULMONARY FUNCTION FILTER (K062913)Sdi Diagnostics, Inc.2007-01-26
FLOSENSE II, MODEL 29-8040 (K033939)Sdi Diagnostics, Inc.2004-01-30
SPIROTEL, MODEL 29-1020 (K031643)Sdi Diagnostics, Inc.2003-12-09
SPIROLAB II, MODEL 29 (K013812)Sdi Diagnostics, Inc.2002-02-11
SDI SB OFFICE, MODEL 29- (K011470)Sdi Diagnostics, Inc.2001-10-12
FLOSENSE, MODEL 29-8010 (K990962)Sdi Diagnostics, Inc.2000-01-07
PULMOGUARD DISPOSABLE BATERIAL/VIRAL FILTER (K934509)Sdi Diagnostics, Inc.1993-10-21

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Every clearance here is in the API, with alerts when new ones post.