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 Fork, Tuning
510(k) Number K874966
Device Name TUNING FORKS
Applicant
Solway, Inc.
Post Office Box 7647
Hollywood,  FL  33081
Applicant Contact MARTIN MUNZER
Correspondent
Solway, Inc.
Post Office Box 7647
Hollywood,  FL  33081
Correspondent Contact MARTIN MUNZER
Regulation Number882.1525
Classification Product Code
GWX  
Date Received12/02/1987
Decision Date 01/04/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-