• 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
510(k) Number K864682
Device Name SALT CREEK P.I. TRAY
Applicant
Salt Creek Medical Technologies
5509 Middletown Rd.
Canfield,  OH  44406
Applicant Contact HOWARD MEADE
Correspondent
Salt Creek Medical Technologies
5509 Middletown Rd.
Canfield,  OH  44406
Correspondent Contact HOWARD MEADE
Date Received12/02/1986
Decision Date 01/06/1987
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-