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 Stethoscope, Manual
510(k) Number K940578
Device Name MANUAL STETOSCOPE
Applicant
Bhs Intl., Inc.
2431 Crofton Ln., Suite 9
Crofton,  MD  21114
Applicant Contact HEATHER WALLACE
Correspondent
Bhs Intl., Inc.
2431 Crofton Ln., Suite 9
Crofton,  MD  21114
Correspondent Contact HEATHER WALLACE
Regulation Number870.1875
Classification Product Code
LDE  
Date Received02/08/1994
Decision Date 04/26/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-