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 Cable, Transducer And Electrode, Patient, (Including Connector)
510(k) Number K933649
Device Name CONMED ECG PATIENT CABLES AND LEADWIRES
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501 -1203
Applicant Contact MARTIN P FORTE, JR.
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501 -1203
Correspondent Contact MARTIN P FORTE, JR.
Regulation Number870.2900
Classification Product Code
DSA  
Date Received07/27/1993
Decision Date 02/18/1994
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
-
-