Mask, Oxygen, Nonbreathing

FDA 510(k) K781414 · Vitalab Products Corp.

Substantially Equivalent

510(k) numberK781414

Submission

Device name
Mask, Oxygen, Nonbreathing
Applicant
Vitalab Products Corp.
Walker, MI, US
Received
August 15, 1978
Decision date
September 7, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KGB – Mask, Oxygen, Non-Rebreathing
Device class
Class I (low risk)
Regulation
21 CFR 868.5570
Specialty
Anesthesiology

Other 510(k)s with product code KGB

510(k)DeviceApplicantDecision
K970688Pocket RescueKGB · Traditional Cheen Houng Ent. Co. , Ltd.09/26/1997SE
K960401Ultimate SealKGB · Traditional Hans Rudolph, Inc.06/20/1996SE
K941336Combo MaskKGB · Traditional Gam Industries, Inc.09/09/1994SE
K935917Challenge Powder-Free, Hypoallergenic, Synthetic Surgical GlovesKGB · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic02/04/1994SE
K932347Compact MaskKGB · Traditional Vital Signs, Inc.01/10/1994SE
K933583Nonrebreathing ValveKGB · Traditional Hans Rudolph, Inc.01/03/1994SE
K933048Laerdal(Tm) Pocket Mask, ModificationKGB · Traditional Laerdal Medical Corp.12/02/1993SE
K930336Profast(R)-Denture Adhesive CreamKGB · Traditional Fittydent-Altwirth & Schmitt GmbH08/24/1993SE
K913164Non Rebreathing MaskKGB · Traditional Specialty Packaging Producs, Inc.01/15/1992SE
K883766Mouth-To-Mask Ventilatory AdjunctKGB · Traditional Medic One10/21/1988SE

More from Medic One

510(k)DeviceDecision
K781416Tubing, Flexible, Medical GasBYX · Traditional 09/11/1978SE
K781415Cannula, Nasal, OxygenCAT · Traditional 09/07/1978SE
K781413Mask, PxygenDPT · Traditional 09/07/1978SE

Questions and answers

When was Mask, Oxygen, Nonbreathing cleared by the FDA?

Mask, Oxygen, Nonbreathing (K781414) received a 510(k) decision of Substantially Equivalent on September 7, 1978, 23 days after the submission was received.

What is the product code of K781414?

The FDA product code is KGB – Mask, Oxygen, Non-Rebreathing, a Class I (low risk) device regulated under 21 CFR 868.5570.