• 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 Grid, Radiographic
510(k) Number K926261
Device Name JPI ALUMINUM INTERSPACED X-RAY GRID
Applicant
Jpi, Inc.
350-J Central Ave.
Bohemia,  NY  11716
Applicant Contact WILLIAM HAGUE
Correspondent
Jpi, Inc.
350-J Central Ave.
Bohemia,  NY  11716
Correspondent Contact WILLIAM HAGUE
Regulation Number892.1910
Classification Product Code
IXJ  
Date Received12/18/1992
Decision Date 03/18/1993
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
-
-