• 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 solid state x-ray imager (flat panel/digital imager)
510(k) Number K140551
Device Name PERKINELMER, XRPAD 4336 MED FLAT PANEL DETECTOR
Applicant
PERKINELMER, INC.
940 WINTER STREET
WALTHAM,  MA  02451
Applicant Contact DAWN SPOONER
Correspondent
PERKINELMER, INC.
940 WINTER STREET
WALTHAM,  MA  02451
Correspondent Contact DAWN SPOONER
Regulation Number892.1680
Classification Product Code
MQB  
Date Received03/04/2014
Decision Date 08/01/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-