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FDA 510(k)

SUPER FLOSSER

K-Number: K874471 · 1988-01-28

ApplicantU.S. Pacific Corp.
Decision Date1988-01-28
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPER FLOSSER is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Pacific Corp.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K874471. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER FLOSSER?

SUPER FLOSSER is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is U.S. Pacific Corp.. The 510(k) number is K874471.

When did SUPER FLOSSER receive FDA 510(k) clearance?

SUPER FLOSSER received FDA 510(k) clearance on 1988-01-28, under 510(k) number K874471.

Who is the listed applicant for SUPER FLOSSER?

The FDA 510(k) record lists U.S. Pacific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER FLOSSER?

The FDA product code for SUPER FLOSSER is JES.

Related Clinical Trials

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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Related Devices (Code: JES)

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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