Pharmajet, Inc. is one of 21653 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pharmajet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATI, PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM, PHARMAJET NEEDLE-FREE INJECTION SYSTEM
3
Total
3
Cleared
0
Denied
Pharmajet, Inc. has 3 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 3 cleared submissions from 2009 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pharmajet, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pharmajet, Inc.
3 devices
Cleared
Jul 27, 2011
PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS...
General Hospital
55d
Cleared
Mar 02, 2011
PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
General Hospital
14d
Cleared
Feb 26, 2009
PHARMAJET NEEDLE-FREE INJECTION SYSTEM
General Hospital
269d