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FDA 510(k)

TRINITY WRINKLE REMOVER

K-Number: K120560 · 2012-11-06

ApplicantCarol Cole Company
Decision Date2012-11-06
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRINITY WRINKLE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Carol Cole Company. It received FDA 510(k) clearance on 2012-11-06 under 510(k) number K120560. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRINITY WRINKLE REMOVER?

TRINITY WRINKLE REMOVER is a medical device that received FDA 510(k) clearance on 2012-11-06. The listed applicant is Carol Cole Company. The 510(k) number is K120560.

When did TRINITY WRINKLE REMOVER receive FDA 510(k) clearance?

TRINITY WRINKLE REMOVER received FDA 510(k) clearance on 2012-11-06, under 510(k) number K120560.

Who is the listed applicant for TRINITY WRINKLE REMOVER?

The FDA 510(k) record lists Carol Cole Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRINITY WRINKLE REMOVER?

The FDA product code for TRINITY WRINKLE REMOVER is OHS.

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Other records listing Carol Cole Company as applicant

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Related Devices (Code: OHS)

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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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