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 K990266
Device Name MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE
Applicant
MICROMEDICAL INDUSTRIES, LTD.
189 HAPP RD.
NORTHFIELD,  IL  60093
Applicant Contact DEAN E SYNDER
Correspondent
MICROMEDICAL INDUSTRIES, LTD.
189 HAPP RD.
NORTHFIELD,  IL  60093
Correspondent Contact DEAN E SYNDER
Classification Product Code
LOS
Date Received01/28/1999
Decision Date 02/02/1999
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-