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FDA 510(k)

PHYSIO-DYNE EASI - LAB

K-Number: K922660 · 1993-04-08

ApplicantPhysio-Dyne
Decision Date1993-04-08
Product CodeBZL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHYSIO-DYNE EASI - LAB is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Dyne. It received FDA 510(k) clearance on 1993-04-08 under 510(k) number K922660. The device is classified under product code BZL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIO-DYNE EASI - LAB?

PHYSIO-DYNE EASI - LAB is a medical device that received FDA 510(k) clearance on 1993-04-08. The listed applicant is Physio-Dyne. The 510(k) number is K922660.

When did PHYSIO-DYNE EASI - LAB receive FDA 510(k) clearance?

PHYSIO-DYNE EASI - LAB received FDA 510(k) clearance on 1993-04-08, under 510(k) number K922660.

Who is the listed applicant for PHYSIO-DYNE EASI - LAB?

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

What is the FDA product code for PHYSIO-DYNE EASI - LAB?

The FDA product code for PHYSIO-DYNE EASI - LAB is BZL.

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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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