ClearanceBrief
Company ยท US

Sequal Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2010. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAWGenerator, Oxygen, Portable7

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 29, 2010K100920MESA II OXYGEN CONCENTRATOR MODEL: T2000 SERIES
Sequal Technologies Co., Ltd., TW
CAW
Dec 31, 2009K091541MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES
Sequal Technologies Co., Ltd., TW
CAW
Oct 20, 2009K083163OMNI 2 OXYGEN SYSTEM
Sequal Technologies, Inc.
CAW
Sep 10, 2004K042262INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10
Sequal Technologies, Inc.
CAW
Mar 27, 2002K013931OMNI OXYGEN SYSTEM, MODEL 1000
Sequal Technologies, Inc.
CAW
Jun 4, 2001K003472INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OM
Sequal Technologies, Inc.
CAW

Latest recalls

DateFirm and productCodeLinked 510(k)
Dec 23, 2009Sequal Technologies Inc
SeQual Technologies Inc. Eclipse Oxygen System, Model 1000 Indicated for the administration of supplemental oxygen.
Terminated
CAWK013931
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