FDA 510(k) Applications Submitted by HOWARD K MANN

FDA 510(k) Number Submission Date Device Name Applicant
K100160 01/20/2010 ZZOMA POSITIONAL SLEEPER MODEL 001 SLEEP SPECIALISTS, LLC
K061689 06/15/2006 AQUATINE EC ENDODONTIC CLEANSER PURICORE, INC.
K071677 06/19/2007 SRT II MUSCLE STIMULATOR THERAPEUTIC INNOVATIONS, INC.
K072500 09/05/2007 ONE STEP HCG URINE/SERUM TEST Guangzhou Wondfo Biotech Co., Ltd.
K013280 10/02/2001 STERILOX LIQUID CHEMICAL STERILANT SYSTEM STERILOX TECHNOLOGIES, INC.
K093175 10/08/2009 WONDFO ONE STEP BUPRENORPHINE URINE TEST, OXYCODONE URINE TEST, PROPOXPHENE URINE TEST, MULTIPLE DRUG OF ABUSE URINE TES Guangzhou Wondfo Biotech Co., Ltd.
K063159 10/17/2006 STERILOX LIQUID CHEMICAL STERILANT SYSTEM PURICORE, INC.
K043443 12/14/2004 ONE STEP HCG URINE PREGNANCY TEST Guangzhou Wondfo Biotech Co., Ltd.
K050024 01/05/2005 ONE STEP MULTIPLE DRUGS OF ABUSE ASSAYS Guangzhou Wondfo Biotech Co., Ltd.
K060901 04/03/2006 VASHE WOUND CLEANSING SYSTEM STERILOX TECHNOLOGIES, INC.
K963428 08/30/1996 UMBILICAL CLAMP AND CUTTER R.O.S.T. MEDICAL DEVELOPMENT, INC.


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