• 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 kit, test, pregnancy, hcg, over the counter
510(k) Number K945846
Device Name ADVANCE(R) PREGNANCY TEST
Applicant
ADVANCED CARE PRODUCTS
ROUTE 202
raritan,  NJ  08869
Applicant Contact marylou panico
Correspondent
ADVANCED CARE PRODUCTS
ROUTE 202
raritan,  NJ  08869
Correspondent Contact marylou panico
Regulation Number862.1155
Classification Product Code
LCX  
Date Received11/30/1994
Decision Date 01/27/1995
Decision substantially equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-