Fraser Harlake Hope III Resuscitator

FDA 510(k) K841496 · Fraser Harlake, Inc.

Substantially Equivalent

510(k) numberK841496

Submission

Device name
Fraser Harlake Hope III Resuscitator
Applicant
Fraser Harlake, Inc.
Mchenry, IL, US
Received
April 10, 1984
Decision date
April 24, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTM – Ventilator, Emergency, Manual (Resuscitator)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5915
Specialty
Anesthesiology
Life-sustaining
Yes

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More from A Plus Medical

510(k)DeviceDecision
K841903Fraser Harlake Emerg. Care Suction SysBTA · Traditional 06/14/1984SE
K833799Sphygomano MeterDXN · Traditional 05/14/1984SE
K833692Fraser Harlake Dental Anti-Polution SysCBN · Traditional 11/29/1983SE
K833151Boyle System Anesthesia Gas MachineBSZ · Traditional 11/14/1983SE
K831427Cyprane Tec 4 Continuous Flow Vapor.CAD · Traditional 07/07/1983SE
K822040Powered Emergency VentilatorCBK · Traditional 08/19/1982SE
K821744Fraser Harlake Nitronox ScavengerCBN · Traditional 06/25/1982SE
K802943Positive End Expiratory Pressure ValveBYE · Traditional 01/15/1981SE

Questions and answers

When was Fraser Harlake Hope III Resuscitator cleared by the FDA?

Fraser Harlake Hope III Resuscitator (K841496) received a 510(k) decision of Substantially Equivalent on April 24, 1984, 14 days after the submission was received.

What is the product code of K841496?

The FDA product code is BTM – Ventilator, Emergency, Manual (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5915.