Magnashield CPR Mouth Barrier

FDA 510(k) K933756 · Cal West Trading Co.

Substantially Equivalent

510(k) numberK933756

Submission

Device name
Magnashield CPR Mouth Barrier
Applicant
Cal West Trading Co.
Orange, CA, US
Received
August 3, 1993
Decision date
January 5, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CBP – Valve, Non-Rebreathing
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5870
Specialty
Anesthesiology
Life-sustaining
Yes

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K152521Seal Rite Non-Rebreathing ValveCBP · Traditional The Lifeguard Store, Inc.06/03/2016SE
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K132143Exhalation ValveCBP · Traditional Intersurgical Incorporated06/04/2014SE

More from Intersurgical Incorporated

510(k)DeviceDecision
K9503924-O2 Plus (CPR) Mouth Barrier, Catalog No. 08050CBP · Traditional 02/21/1995SE
K920269Ez Gauze SpongeNAB · Traditional 04/22/1992SE
K914842Gauze Bandage RollNAB · Traditional 12/04/1991SE
K912952Bandage CompressNAB · Traditional 10/04/1991SE
K912950Compress DressingNAB · Traditional 10/04/1991SE
K912953Gauze CompressNAB · Traditional 09/30/1991SE
K912955Eye PadEFQ · Traditional 09/10/1991SE
K912954Stretch Gauze BandageNAB · Traditional 09/10/1991SE
K91295112-PLY Gauze PadNAB · Traditional 09/10/1991SE
K912949Triangular BANDAGE,40NAB · Traditional 09/06/1991SE

Questions and answers

When was Magnashield CPR Mouth Barrier cleared by the FDA?

Magnashield CPR Mouth Barrier (K933756) received a 510(k) decision of Substantially Equivalent on January 5, 1994, 155 days after the submission was received.

What is the product code of K933756?

The FDA product code is CBP – Valve, Non-Rebreathing, a Class II (moderate risk) device regulated under 21 CFR 868.5870.