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510(k) K930786

Device
EPCOR
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
510(k) number
K930786
Product code
DRW  
Decision
Substantially Equivalent (SESE)
Decision date
1994-09-26
Date received
1993-02-16
Regulation
870.2350
Classification name
Adaptor, Lead Switching, Electrocardiograph
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
KATHLEEN RUTHERFORD
Address
186 Wood Ave. S. Iselin NJ US 08830 08830

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code DRW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K033513EASI ECG ALGORITHMPhilips Medical Systems2004-01-15
K020456EASI 12 LEAD ALGORITHMPhilips Medical Systems2002-07-09
K872781EASI LEAD SYSTEM CABLE ASSEMBLYTotemite Medical Electronics1987-12-29
K861981ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTORVital Signs, Inc.1986-08-25
K851627KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTREaton Medical Group1985-11-08
K851632PCX-100 PATIENT INPUT LEADWIREEaton Medical Group1985-11-08
K761210LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)Physio-Control Corp.1976-12-21

Legacy Summary#

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FDA Review#

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