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FDA 510(k)

PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE)

K-Number: K892670 · 1989-09-22

ApplicantPhysio-Dyne Instrument Corp.
Decision Date1989-09-22
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE) is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Dyne Instrument Corp.. It received FDA 510(k) clearance on 1989-09-22 under 510(k) number K892670. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE)?

PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE) is a medical device that received FDA 510(k) clearance on 1989-09-22. The listed applicant is Physio-Dyne Instrument Corp.. The 510(k) number is K892670.

When did PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE) receive FDA 510(k) clearance?

PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE) received FDA 510(k) clearance on 1989-09-22, under 510(k) number K892670.

Who is the listed applicant for PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE)?

The FDA 510(k) record lists Physio-Dyne Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE)?

The FDA product code for PHYSIO-DYNE EASI (EASY ANALOG SAMPLING INTERFACE) is BZC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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