Del Mar Model 750 Innovator Holter Management Syst

FDA 510(k) K860470 · Del Mar Avionics

Substantially Equivalent

510(k) numberK860470

Submission

Device name
Del Mar Model 750 Innovator Holter Management Syst
Applicant
Del Mar Avionics
Irvine, CA, US
Received
February 6, 1986
Decision date
April 30, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSI – Detector And Alarm, Arrhythmia
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1025
Specialty
Cardiovascular

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More from Memtec Corporation

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K990027Omnicorder, Model 464DSH · Abbreviated 02/09/1999SE
K971696Sentinel Recorder, Models 471/472DXH · Traditional 12/30/1997SE
K963174Holter Digicorder with Pacer Option (Model 483)DSH · Traditional 03/13/1997SE
K950020Holter Pacercorder(R)DSH · Traditional 08/17/1995SE
K942653Holter SSR Digicorder(Tm)DSH · Traditional 05/10/1995SE
K922221Sprint DX, Model 5400 Exercise Stress Test SystemLOS · Traditional 04/21/1993SE
K896862Model 263 Spectrascan(Tm) Holter Analysis SystemDSI · Traditional 04/18/1990SE
K895793Micropotential Analyzer/Spectrocardiography OptionDSH · Traditional 02/13/1990SE
K894543Model 493 SSR-3 Three Channel Solid-State RecorderDSI · Traditional 02/08/1990SE
K891148Model 152 Delta Holter ECG Analysis SystemDSI · Traditional 05/11/1989SE

Questions and answers

When was Del Mar Model 750 Innovator Holter Management Syst cleared by the FDA?

Del Mar Model 750 Innovator Holter Management Syst (K860470) received a 510(k) decision of Substantially Equivalent on April 30, 1986, 83 days after the submission was received.

What is the product code of K860470?

The FDA product code is DSI – Detector And Alarm, Arrhythmia, a Class II (moderate risk) device regulated under 21 CFR 870.1025.