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FDA 510(k)

INTIMOL

K-Number: K061466 · 2006-12-04

ApplicantDlc Laboratories, Inc.
Decision Date2006-12-04
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTIMOL is the device name listed in this FDA 510(k) record. The listed applicant is Dlc Laboratories, Inc.. It received FDA 510(k) clearance on 2006-12-04 under 510(k) number K061466. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTIMOL?

INTIMOL is a medical device that received FDA 510(k) clearance on 2006-12-04. The listed applicant is Dlc Laboratories, Inc.. The 510(k) number is K061466.

When did INTIMOL receive FDA 510(k) clearance?

INTIMOL received FDA 510(k) clearance on 2006-12-04, under 510(k) number K061466.

Who is the listed applicant for INTIMOL?

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

What is the FDA product code for INTIMOL?

The FDA product code for INTIMOL is NUC.

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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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