ELECTRODE CABLE

Cable, Transducer And Electrode, Patient, (including Connector)

VITAL CONNECTIONS, INC.

The following data is part of a premarket notification filed by Vital Connections, Inc. with the FDA for Electrode Cable.

Pre-market Notification Details

• Device ID: K880320
• 510k Number: K880320
• Device Name: ELECTRODE CABLE
• Classification: Cable, Transducer And Electrode, Patient, (including Connector)
• Applicant: VITAL CONNECTIONS, INC. 955 N. THIRD ST. Tipp City, OH 45371
• Contact: Mark L Meister
• Correspondent: Mark L Meister; VITAL CONNECTIONS, INC. 955 N. THIRD ST. Tipp City, OH 45371
• Product Code: DSA
• CFR Regulation Number: 870.2900 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1988-01-26
• Decision Date: 1988-03-22

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00816943022173	K880320	000
00816943022166	K880320	000
00884838001862	K880320	000