• 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 Chair, Positioning, Electric
510(k) Number K851218
Device Name PENOX LIFT CHAIR
Applicant
Penox Technologies, Inc.
One Penox Plz., Commerce Rd.
P.O. Box 785
Pittston,  PA  18640
Applicant Contact ALAN P SCHWARTZ
Correspondent
Penox Technologies, Inc.
One Penox Plz., Commerce Rd.
P.O. Box 785
Pittston,  PA  18640
Correspondent Contact ALAN P SCHWARTZ
Regulation Number890.3110
Classification Product Code
INO  
Date Received03/26/1985
Decision Date 06/21/1985
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
-
-