SEER

Detector And Alarm, Arrhythmia

MARQUETTE ELECTRONICS, INC.

The following data is part of a premarket notification filed by Marquette Electronics, Inc. with the FDA for Seer.

Pre-market Notification Details

• Device ID: K882818
• 510k Number: K882818
• Device Name: SEER
• Classification: Detector And Alarm, Arrhythmia
• Applicant: MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223
• Contact: Thomas Massopust
• Correspondent: Thomas Massopust; MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223
• Product Code: DSI
• CFR Regulation Number: 870.1025 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1988-07-08
• Decision Date: 1989-06-22