• 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 Table, Mechanical
510(k) Number K901375
Device Name GRASP (GRIGG-RUSSEL AIR SUPPORT PILLOW)
Applicant
Medical Plastics Laboratory, Inc.
816 Dixie Ave.
Florence,  AL  35630
Applicant Contact ELLEN S GRIGG
Correspondent
Medical Plastics Laboratory, Inc.
816 Dixie Ave.
Florence,  AL  35630
Correspondent Contact ELLEN S GRIGG
Regulation Number890.3750
Classification Product Code
INW  
Date Received03/22/1990
Decision Date 04/19/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-