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FDA 510(k)

K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING

K-Number: K062535 · 2007-01-26

ApplicantMcneil-Ppc, Inc.
Decision Date2007-01-26
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING is the device name listed in this FDA 510(k) record. The listed applicant is Mcneil-Ppc, Inc.. It received FDA 510(k) clearance on 2007-01-26 under 510(k) number K062535. 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 K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING?

K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING is a medical device that received FDA 510(k) clearance on 2007-01-26. The listed applicant is Mcneil-Ppc, Inc.. The 510(k) number is K062535.

When did K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING receive FDA 510(k) clearance?

K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING received FDA 510(k) clearance on 2007-01-26, under 510(k) number K062535.

Who is the listed applicant for K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING?

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

What is the FDA product code for K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING?

The FDA product code for K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING is NUC.

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Other records listing Mcneil-Ppc, Inc. as applicant

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.

K081236K-Y BRAND INTRIGUE 2-IN-1 MASSAGE CREMEK072421K-Y BRAND YOURS+MINEK072360K-Y BRAND INTRIGUE INTENSE WARMING SENSATIONK053397K-Y BRAND SENSUAL MISTK023789O.B. TAMPONS

Related Devices (Code: NUC)

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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