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FDA 510(k)

FREEDOM, MODEL 4660

K-Number: K001023 · 2000-09-22

ApplicantJohnson & Johnson Consumer Companies, Inc.
Decision Date2000-09-22
Product CodeSEJ
DecisionSubstantially Equivalent

Device Summary

FREEDOM, MODEL 4660 is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Consumer Companies, Inc.. It received FDA 510(k) clearance on 2000-09-22 under 510(k) number K001023. The device is classified under product code SEJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM, MODEL 4660?

FREEDOM, MODEL 4660 is a medical device that received FDA 510(k) clearance on 2000-09-22. The listed applicant is Johnson & Johnson Consumer Companies, Inc.. The 510(k) number is K001023.

When did FREEDOM, MODEL 4660 receive FDA 510(k) clearance?

FREEDOM, MODEL 4660 received FDA 510(k) clearance on 2000-09-22, under 510(k) number K001023.

Who is the listed applicant for FREEDOM, MODEL 4660?

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

What is the FDA product code for FREEDOM, MODEL 4660?

The FDA product code for FREEDOM, MODEL 4660 is SEJ.

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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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