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 General Surgery Tray
510(k) Number K872011
Device Name PORT ACCESS KITS
Applicant
The Jarid Group, Inc.
41 Ascot Dr.
Wayside,  NJ  07712
Applicant Contact JOEL A MARCUS
Correspondent
The Jarid Group, Inc.
41 Ascot Dr.
Wayside,  NJ  07712
Correspondent Contact JOEL A MARCUS
Regulation Number878.4370
Classification Product Code
LRO  
Date Received05/26/1987
Decision Date 07/13/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-