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 Counter (Beta, Gamma) For Clinical Use
510(k) Number K780383
Device Name COUNTER, RADIOASSAY, AUTO., MICROMEDIC
Applicant
Micromedic Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Micromedic Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.2320
Classification Product Code
JJJ  
Date Received03/09/1978
Decision Date 03/22/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-