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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