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FDA 510(k)

HYDRO FLOSS

K-Number: K923937 · 1994-02-25

ApplicantHydro Floss, Inc.
Decision Date1994-02-25
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDRO FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Hydro Floss, Inc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K923937. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRO FLOSS?

HYDRO FLOSS is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Hydro Floss, Inc.. The 510(k) number is K923937.

When did HYDRO FLOSS receive FDA 510(k) clearance?

HYDRO FLOSS received FDA 510(k) clearance on 1994-02-25, under 510(k) number K923937.

Who is the listed applicant for HYDRO FLOSS?

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

What is the FDA product code for HYDRO FLOSS?

The FDA product code for HYDRO FLOSS is EFS.

Related Clinical Trials

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Related Devices (Code: EFS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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