Awareness Technology, Inc.
Awareness Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 2018.
Top product codes for Awareness Technology, Inc.
Recent clearances by Awareness Technology, Inc.
- K171476 — SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-)
- K013420 — CHEMWELL, ALSO KNOWN AS PROJECT 2900
- K010877 — CHEMWELL, MODEL 2900
- K974762 — STAT TRACKS
- K943729 — DYE CHECK STRIPS 545-630
- K941394 — STAT FAX 2600
- K923598 — REDI-CHECK PHOTMETER Q.A.
- K900224 — STAT FAX(TM)-2100
- K892656 — DRI-DYE CHECK STRIPS (TM)-405
- K882938 — STAT FAX(TM)
- K873451 — PROJECT 300 MICROASSAY BP-12, EIA MINILAB
- K871679 — FOCUS-GHB
- K864634 — AP1 COLORIMETER
- K861697 — SELF ASSURE/GHB (CAPILLARY-BLOOD COLLECTION KIT)
- K851467 — HEMOGLOBIN ANALYZER
- K850994 — SPECTRA 1 FILTER PHOTOMETER
- K850995 — SMART ALEX COMPACT CLINICAL ANALYZER(CCA)(FILTER P
- K850993 — SMART ALEX II MULTI-FILTER PHOTOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.