FDA 510(k)

AUDIOMETER DA 323

K-Number: K933222 · 1993-11-01

ApplicantFuturemed Div. of Future Impex Corp.

Decision Date1993-11-01

Product CodeEWO

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

AUDIOMETER DA 323 is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K933222. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUDIOMETER DA 323?

AUDIOMETER DA 323 is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K933222.

When did AUDIOMETER DA 323 receive FDA 510(k) clearance?

AUDIOMETER DA 323 received FDA 510(k) clearance on 1993-11-01, under 510(k) number K933222.

Who is the listed applicant for AUDIOMETER DA 323?

The FDA 510(k) record lists Futuremed Div. of Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUDIOMETER DA 323?

The FDA product code for AUDIOMETER DA 323 is EWO.

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Official Source

View on FDA Database →

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