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FDA 510(k)

SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET

K-Number: K900991 · 1990-05-15

ApplicantTocad America, Inc.
Decision Date1990-05-15
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET is the device name listed in this FDA 510(k) record. The listed applicant is Tocad America, Inc.. It received FDA 510(k) clearance on 1990-05-15 under 510(k) number K900991. 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 SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET?

SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Tocad America, Inc.. The 510(k) number is K900991.

When did SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET receive FDA 510(k) clearance?

SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET received FDA 510(k) clearance on 1990-05-15, under 510(k) number K900991.

Who is the listed applicant for SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET?

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

What is the FDA product code for SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET?

The FDA product code for SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET is EFS.

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Related Devices (Code: EFS)

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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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