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FDA 510(k)

FLOSSAGE - ELECTRIC TOOTHFLOSSER

K-Number: K850562 · 1985-03-27

ApplicantMcspadden, Inc.
Decision Date1985-03-27
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSSAGE - ELECTRIC TOOTHFLOSSER is the device name listed in this FDA 510(k) record. The listed applicant is Mcspadden, Inc.. It received FDA 510(k) clearance on 1985-03-27 under 510(k) number K850562. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOSSAGE - ELECTRIC TOOTHFLOSSER?

FLOSSAGE - ELECTRIC TOOTHFLOSSER is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Mcspadden, Inc.. The 510(k) number is K850562.

When did FLOSSAGE - ELECTRIC TOOTHFLOSSER receive FDA 510(k) clearance?

FLOSSAGE - ELECTRIC TOOTHFLOSSER received FDA 510(k) clearance on 1985-03-27, under 510(k) number K850562.

Who is the listed applicant for FLOSSAGE - ELECTRIC TOOTHFLOSSER?

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

What is the FDA product code for FLOSSAGE - ELECTRIC TOOTHFLOSSER?

The FDA product code for FLOSSAGE - ELECTRIC TOOTHFLOSSER is JEQ.

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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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