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 Camera, Scintillation (Gamma)
510(k) Number K780155
Device Name DUAL CHANNEL PULSE HEIGHT ANALYZER
Applicant
Iso Graphics, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Iso Graphics, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number892.1100
Classification Product Code
IYX  
Date Received01/30/1978
Decision Date 03/02/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-