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 K837029
Device Name ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE
Applicant
American Electromedics Corp.
13 Sagamore Park Rd.
Hudson,  NH  03051
Correspondent
American Electromedics Corp.
13 Sagamore Park Rd.
Hudson,  NH  03051
Date Received12/10/1982
Decision Date 03/22/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-