• 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 Radioimmunoassay, Phencyclidine
510(k) Number K913864
Device Name PCP DIRECT RIA KIT (I-125)
Applicant
Immunalysis Corporation
1707 Gardena Ave.
Glendale,  CA  91204
Applicant Contact JAMES R SOARES
Correspondent
Immunalysis Corporation
1707 Gardena Ave.
Glendale,  CA  91204
Correspondent Contact JAMES R SOARES
Classification Product Code
LCL  
Date Received08/27/1991
Decision Date 10/11/1991
Decision Substantially Equivalent (SESE)
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-