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FDA 510(k)

SNORKEL

K-Number: K112766 · 2012-06-04

ApplicantFellmar Company
Decision Date2012-06-04
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORKEL is the device name listed in this FDA 510(k) record. The listed applicant is Fellmar Company. It received FDA 510(k) clearance on 2012-06-04 under 510(k) number K112766. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNORKEL?

SNORKEL is a medical device that received FDA 510(k) clearance on 2012-06-04. The listed applicant is Fellmar Company. The 510(k) number is K112766.

When did SNORKEL receive FDA 510(k) clearance?

SNORKEL received FDA 510(k) clearance on 2012-06-04, under 510(k) number K112766.

Who is the listed applicant for SNORKEL?

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

What is the FDA product code for SNORKEL?

The FDA product code for SNORKEL is LQZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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