FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

PASR/QUIETNITE

K Number: K093340 · Decision Jun 11, 2010
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
1
Review Days
228

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Basic Information

Device Name
PASR/QUIETNITE
K Number
K093340
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exact Supplies , Ltd.
Date Received
October 26, 2009
Decision Date
June 11, 2010
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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