FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BREATHE RIGHT NASAL STRIP

K Number: K955711 · Decision May 30, 1996
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
19
Applicant Total
14
Review Days
164

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Basic Information

Device Name
BREATHE RIGHT NASAL STRIP
K Number
K955711
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3900
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cns, Inc.
Date Received
December 18, 1995
Decision Date
May 30, 1996
Product Code
LWF
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
LWF Dilator, Nasal

Similar 510(k) Clearances

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

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Other Clearances by Cns, Inc.

K Number Device Name
K954914 BREATHE RIGHT NASAL STRIP
K953772 BREATHE RIGHT NASAL STRIP
K950273 SLEEP TEST(TM)
K921220 BREATHE RIGHT
K912436 AM-PAK
K904432 SLEEP I/T-5 AND SLEEP I/T-8
K910452 RESPI-PAK RT-PAK
K901549 CNS SATELLITE 100, 200, 1000, 2000 ELECTROENCE.
K897107 POLY G PHYSIOLOGICAL DATA RECORDER
K860829 CNS 4/8 AND CT 48.1 SOFTWARE
Search all 14 clearances from Cns, Inc. →