ClearanceBrief
Company ยท US

Viratek, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1990. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BYLTent, Oxygen2
CAFNebulizer (Direct Patient Interface)2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 9, 1990K896608SPAG PAK
Viratek, Inc.
BYL
Aug 1, 1988K882396AEROSOL DELIVERY HOOD
Viratek, Inc.
BYL
Oct 6, 1987K871427(SPAG) MODEL SPAG-2 6000 SERIES
Viratek, Inc.
CAF
Oct 6, 1987K870051SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE
Viratek, Inc.
CAF
Dec 30, 1985K843717VIRATEK SMALL PARTICLE AEROSOL GENERAT
Viratek, Inc.

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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