FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ZQUIET-SA

K Number: K140777 · Decision Jul 25, 2014
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
6
Review Days
119

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Basic Information

Device Name
ZQUIET-SA
K Number
K140777
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sleeping Well, LLC
Date Received
March 28, 2014
Decision Date
July 25, 2014
Product Code
LRK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRK Device, Anti-Snoring

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Other Clearances by Sleeping Well, LLC

K Number Device Name
K213088 ZQuiet Advance
K180124 ZQuiet
K122475 ZQUIET PRO-PLUS
K093407 ZQUIET MOUTHPIECE
K090503 ZQUIET MOUTHPIECE