Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Atomic Absorption, Lithium
510(k) Number K912244
Device Name UROTEST GPH
Applicant
In Wha Pharmaceutical Co., Ltd.
Buk-Ku Chungchun-Dong 234-1
Korea,  KR
Correspondent
In Wha Pharmaceutical Co., Ltd.
Buk-Ku Chungchun-Dong 234-1
Korea,  KR
Regulation Number862.3560
Classification Product Code
JII  
Date Received05/21/1991
Decision Date 11/22/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-