ClearanceBrief
Company ยท US

Bioject, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 2009. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KZEInjector, Fluid, Non-Electrically Powered7
LHISet, I.V. Fluid Transfer2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 2, 2009K090003ZETAJET
Bioject, Inc.
KZE
Jun 3, 2005K050734COOL.CLICK
Bioject, Inc.
KZE
Apr 5, 2001K010623RECONSTITUTION KIT & VIAL CONNECTOR
Bioject, Inc.
LHI
Mar 8, 2001K003908SEROJET
Bioject, Inc.
KZE
Jun 22, 2000K994384CLICKER
Bioject, Inc.
KZE
Mar 5, 1997K960373BIOJECTOR 2000 MODEL 1B02000
Bioject, Inc.
KZE
Oct 15, 1996K963012BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)
Bioject, Inc.
LHI
Jun 28, 1994K920631BIOJECT JET INJECTION SYSTEM
Bioject, Inc.
KZE
Apr 23, 1987K861687BIOJECTOR SYRINGE SYSTEM
Bioject, Inc.
KZE

Latest recalls

DateFirm and productCodeLinked 510(k)
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