Easy Breathing Nasal Strips

FDA 510(k) K955233 · Corbett Lair, Inc.

Substantially Equivalent

510(k) numberK955233

Submission

Device name
Easy Breathing Nasal Strips
Applicant
Corbett Lair, Inc.
Portland, OR, US
Received
November 14, 1995
Decision date
December 21, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LWF – Dilator, Nasal
Device class
Class I (low risk)
Regulation
21 CFR 874.3900
Specialty
Ear, Nose, Throat

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K982929Maxair Nasal Dilator SystemLWF · Traditional Hnl Technologies09/09/1998SE
K963326Breathe FitLWF · Traditional Cambridge Assoc.02/12/1997SE
K962698Acutek's ClearpasageLWF · Traditional Acutek Adhesive Specialties, Inc.09/09/1996SE
K962400Air Max External Nasal Dilator StripLWF · Traditional American White Cross, Inc.09/09/1996SE
K955711Breathe Right Nasal StripLWF · Traditional Cns, Inc.05/30/1996SE
K954914Breathe Right Nasal StripLWF · Traditional Cns, Inc.02/27/1996SE
K953042E-Z BreathersLWF · Traditional E-Z Kare Good Health Systems, Inc.12/08/1995SE

More from E-Z Kare Good Health Systems, Inc.

510(k)DeviceDecision
K954252Easy Breathing Nasal StripsLWF · Traditional 10/18/1995SE

Questions and answers

When was Easy Breathing Nasal Strips cleared by the FDA?

Easy Breathing Nasal Strips (K955233) received a 510(k) decision of Substantially Equivalent on December 21, 1995, 37 days after the submission was received.

What is the product code of K955233?

The FDA product code is LWF – Dilator, Nasal, a Class I (low risk) device regulated under 21 CFR 874.3900.