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
510(k) Number K854441
Device Name STUART GILMAN'S WEIGHT LOSS PLAN
Applicant
Alpha Therapeutic Corp.
P.O. Box 516
Rouses Point,  NY  12979
Applicant Contact STUART GILMAN
Correspondent
Alpha Therapeutic Corp.
P.O. Box 516
Rouses Point,  NY  12979
Correspondent Contact STUART GILMAN
Classification Product Code
LDQ
Date Received11/05/1985
Decision Date 02/10/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-