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FDA 510(k)

MODEL EB-22 NOISE STIK

K-Number: K895200 · 1990-01-22

ApplicantEckstein Brothers, Inc.
Decision Date1990-01-22
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL EB-22 NOISE STIK is the device name listed in this FDA 510(k) record. The listed applicant is Eckstein Brothers, Inc.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K895200. 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 MODEL EB-22 NOISE STIK?

MODEL EB-22 NOISE STIK is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Eckstein Brothers, Inc.. The 510(k) number is K895200.

When did MODEL EB-22 NOISE STIK receive FDA 510(k) clearance?

MODEL EB-22 NOISE STIK received FDA 510(k) clearance on 1990-01-22, under 510(k) number K895200.

Who is the listed applicant for MODEL EB-22 NOISE STIK?

The FDA 510(k) record lists Eckstein Brothers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL EB-22 NOISE STIK?

The FDA product code for MODEL EB-22 NOISE STIK is EWO.

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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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