CONMED EKG STRIPPER


Device Classification Name

electrode, electrocardiograph

510(k) Number K960264
Device Name CONMED EKG STRIPPER
Applicant
CONMED CORP.
p.o. box 1408
dayton, 
OH 
45401 -1408

Applicant Contact ira d duesler, jr.
Correspondent
CONMED CORP.
p.o. box 1408
dayton, 
OH 
45401 -1408

Correspodent Contact ira d duesler, jr.
Regulation Number 870.2360
Classification Product Code
DRX  
Date Received 01/18/1996
Decision Date 04/09/1996
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

Type Traditional
Reviewed by Third Party No

Combination Product

No