Bear Cub 750 PSV

FDA 510(k) K992788 · Bear Medical Systems, Inc.

Substantially Equivalent

510(k) numberK992788

Submission

Device name
Bear Cub 750 PSV
Applicant
Bear Medical Systems, Inc.
Palm Spring, CA, US
Received
August 19, 1999
Decision date
September 16, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CBK – Ventilator, Continuous, Facility Use
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5895
Specialty
Anesthesiology
Life-sustaining
Yes

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K890724Mofification Bear NVM-1 Neonatal Volume MonitorBZK · Traditional 03/30/1989SE
K882764Bear EVC-100 ControllerCBK · Traditional 09/30/1988SE
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K872660Bear NVM-1BZK · Traditional 02/12/1988SE
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Questions and answers

When was Bear Cub 750 PSV cleared by the FDA?

Bear Cub 750 PSV (K992788) received a 510(k) decision of Substantially Equivalent on September 16, 1999, 28 days after the submission was received.

What is the product code of K992788?

The FDA product code is CBK – Ventilator, Continuous, Facility Use, a Class II (moderate risk) device regulated under 21 CFR 868.5895.