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

SNORE-NO-MORE

K Number: K922818 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
26
Applicant Total
13
Review Days
608

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Basic Information

Device Name
SNORE-NO-MORE
K Number
K922818
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Great Lakes Orthodontics, Ltd.
Date Received
June 11, 1992
Decision Date
February 9, 1994
Product Code
LQZ
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
LQZ Device, Jaw Repositioning

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Other Clearances by Great Lakes Orthodontics, Ltd.

K Number Device Name
K172765 Smart Moves Complete
K150702 Exceed Tx
K083479 BIOCRYL X
K041718 KELES FACEMASK
K040881 METACRYL
K033632 VARIFLEX
K925275 SOFT DENTURE RELINE MATERIAL ELASTOLINE
K870908 STEADY RESIN
K861424 ADAPTABLE CLASS III MASK
K840805 ORAL SAFE
Search all 13 clearances from Great Lakes Orthodontics, Ltd. →