Plotter Model (MP100)

FDA 510(k) K861905 · Madsen Electronics (Canada) , Ltd.

Substantially Equivalent

510(k) numberK861905

Submission

Device name
Plotter Model (MP100)
Applicant
Madsen Electronics (Canada) , Ltd.
Oakville, Ontario, CA
Received
May 16, 1986
Decision date
November 26, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Madsen Electronics (Canada) , Ltd.

510(k)DeviceDecision
K942749Hi-Pro/Noah Universal Hearing InstrumentESD · Traditional 07/18/1994SE
K931325Otoacoustic Emissions Unit Celesta 503EWO · Traditional 02/18/1994SE
K931324Orbiter 922 Clinical AudiometerEWO · Traditional 11/19/1993SE
K910247Zodiac 901 Middle-Ear AnalyzerETY · Traditional 06/19/1991SE
K884372Madsen IGO1500 Insertion Gain OptimizerETW · Traditional 02/13/1989SE
K884371Madsen IGO-HAT1500 Hearing Aid Dispenser SystemETW · Traditional 02/13/1989SE
K883478Diagnostic Audiometer, Model Midimate 602EWO · Traditional 11/17/1988SE
K874354Audiometric Impedance Tester, Model Z02020ETY · Traditional 01/27/1988SE
K870229Hearing Aid Test System Model Hat 1000ETW · Traditional 03/13/1987SE
K854533Single Channel Brain Stem Response Audiometer BSR2 · Traditional 09/30/1986SE

Questions and answers

When was Plotter Model (MP100) cleared by the FDA?

Plotter Model (MP100) (K861905) received a 510(k) decision of Substantially Equivalent on November 26, 1986, 194 days after the submission was received.