Sdi Diagnostics, Inc.
Sdi Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2016.
Top product codes for Sdi Diagnostics, Inc.
Recent clearances by Sdi Diagnostics, Inc.
- K150515 — IQSense Flow Sensor Mouthpiece
- K092813 — ASTRASONIC SPIROMETER, MODEL 29-8000
- K061571 — ASTRA 300
- K062913 — ASTRAGUARD PULMONARY FUNCTION FILTER
- K033939 — FLOSENSE II, MODEL 29-8040
- K031643 — SPIROTEL, MODEL 29-1020
- K013812 — SPIROLAB II, MODEL 29
- K011470 — SDI SB OFFICE, MODEL 29-
- K990962 — FLOSENSE, MODEL 29-8010
- K934509 — PULMOGUARD DISPOSABLE BATERIAL/VIRAL FILTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.