EPCOR

Adaptor, Lead Switching, Electrocardiograph

SIEMENS MEDICAL SOLUTIONS USA, INC.

The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Epcor.

Pre-market Notification Details

• Device ID: K930786
• 510k Number: K930786
• Device Name: EPCOR
• Classification: Adaptor, Lead Switching, Electrocardiograph
• Applicant: SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830
• Contact: Kathleen Rutherford
• Correspondent: Kathleen Rutherford; SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830
• Product Code: DRW
• CFR Regulation Number: 870.2350 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-02-16
• Decision Date: 1994-09-26