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

ZQUIET MOUTHPIECE

K Number: K090503 · Decision Mar 10, 2009
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
6
Review Days
13

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Basic Information

Device Name
ZQUIET MOUTHPIECE
K Number
K090503
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
February 25, 2009
Decision Date
March 10, 2009
Product Code
LRK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

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

Product Code Device Name
LRK Device, Anti-Snoring

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LRK), ordered by most recent decision date.

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Other Clearances by Sleeping Well, LLC

K Number Device Name
K213088 ZQuiet Advance
K180124 ZQuiet
K140777 ZQUIET-SA
K122475 ZQUIET PRO-PLUS
K093407 ZQUIET MOUTHPIECE