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510(k) K112766

SNORKEL by Fellmar Company — Product Code LQZ

K112766 is an FDA 510(k) premarket notification submitted by Fellmar Company for the device "SNORKEL". The FDA issued a decision of Substantially Equivalent on June 4, 2012. The device falls under product code LQZ (Device, Jaw Repositioning), a Class II device regulated under 21 CFR 872.5570.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 4, 2012
Date Received
September 22, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Jaw Repositioning
Device Class
Class II
Regulation Number
872.5570
Review Panel
DE
Submission Type

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FDA data resources