PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE)— 510(k) K892670

Name: FDA 510(k) clearance K892670
Creator: U.S. Food and Drug Administration
Published: 1989-09-22

Substantially Equivalent

Physio-Dyne Instrument Corp.

FDA 510(k) clearance K892670 for PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE), Substantially Equivalent on 1989-09-22. Applicant: Physio-Dyne Instrument Corp.. Device class: 2.

Clearance details

Applicant: Physio-Dyne Instrument Corp.
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 1989-04-13
Decision date: 1989-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Massapequa, NY, US

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