510(k) K981949

Device
NUMOBAG
Applicant
NUMOTECH, INC.
510(k) number
K981949
Product code
KPJ  
Decision
Substantially Equivalent (SESE)
Decision date
1999-02-03
Date received
1998-06-03
Regulation
878.5650
Classification name
Chamber, Oxygen, Topical, Extremity
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
W. PATRICK NOONAN
Address
21800 Oxnard St., Suite 840 Warner Center Plz. Woodland Hills CA US 91367 91367

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KPJ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K250188Wound Treatment System (VHT-200)Vaporox, Inc.2025-03-10
K212121VHT-200 Wound Treatment SystemVaporox, Inc.2023-03-23
K190742EPIFLO-28Neogenix, LLC Dba Ogenix2019-12-13
K112634NATROX TOPICAL OXYGEN DELIVERY SYSTEM WITH IODPInotec Amd , Ltd.2012-07-03
K120764EPIFLO(R)Neogenix, LLC2012-04-27
K090681TANSCU O2Electrochemical Oxygen Concepts, Inc.2009-08-12
K080966HYPER-BOX TOPICAL WOUND OXYGEN SYSTEMAoti , Ltd.2008-08-06
K050156WHS-1000 WOUND HEALING SYSTEMIyia Technologies, Inc.2005-06-17
K023456OXYBOX SYSTEMOxyfast Corporation2003-02-24
K022028VX-400 TOPICAL HYPERBARIC OXYGEN CHAMBERVascular One, Inc.2002-12-17
K020466HEC 1000Metro Medical Equipment, Inc.2002-05-08
K002632OXYGENATORAdjunctive Therapeutics, Inc.2001-10-25
K971507O2 BOOTGwr Medical, Llp1997-11-07
K960756LIFETECH CASSETTELifetech Systems, Inc.1997-08-29
K963777HYPER PULSE INTERMITTENT TOPICAL OXYGEN CHAMBER C-100, CB-100Stephenson Industries, Inc.1997-07-28

Legacy Summary#

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FDA Review#

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