FDA 510(k)

VICKS POWERSHOT DRY THROAT & MOUTH RELIEF

K-Number: K091419 · 2009-08-28

Decision Date2009-08-28

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

VICKS POWERSHOT DRY THROAT & MOUTH RELIEF is the device name listed in this FDA 510(k) record. The listed applicant is The Procter & Gamble Co.. It received FDA 510(k) clearance on 2009-08-28 under 510(k) number K091419. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICKS POWERSHOT DRY THROAT & MOUTH RELIEF?

VICKS POWERSHOT DRY THROAT & MOUTH RELIEF is a medical device that received FDA 510(k) clearance on 2009-08-28. The listed applicant is The Procter & Gamble Co.. The 510(k) number is K091419.

When did VICKS POWERSHOT DRY THROAT & MOUTH RELIEF receive FDA 510(k) clearance?

VICKS POWERSHOT DRY THROAT & MOUTH RELIEF received FDA 510(k) clearance on 2009-08-28, under 510(k) number K091419.

Who is the listed applicant for VICKS POWERSHOT DRY THROAT & MOUTH RELIEF?

The FDA 510(k) record lists The Procter & Gamble Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VICKS POWERSHOT DRY THROAT & MOUTH RELIEF?

The FDA product code for VICKS POWERSHOT DRY THROAT & MOUTH RELIEF is LFD.

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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.