• 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, Examination, Medical, Powered
510(k) Number K864072
Device Name ADEC 1005-C CHAIR
Applicant
Cherne Industries, Inc.
5701 S. County Rd. 18
Minneapolis,  MN  55436
Applicant Contact MARK W KROLL
Correspondent
Cherne Industries, Inc.
5701 S. County Rd. 18
Minneapolis,  MN  55436
Correspondent Contact MARK W KROLL
Regulation Number878.4960
Classification Product Code
LGX  
Date Received10/20/1986
Decision Date 11/07/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-