Suspension 7

FDA 510(k) K843985 · Cgr Medical Corp.

Substantially Equivalent

510(k) numberK843985

Submission

Device name
Suspension 7
Applicant
Cgr Medical Corp.
Columbia, MD, US
Received
October 11, 1984
Decision date
November 5, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Cgr Medical Corp.

510(k)DeviceDecision
K843926Prestilix 1690IXR · Traditional 12/17/1984SE
K843235StenoscopJAA · Traditional 11/08/1984SE
K841649Maximax - 4IZP · Traditional 06/05/1984SE
K833223Sonel 3000AIYO · Traditional 05/09/1984SE
K834306Phasix-High Frequency GeneratorITY · Traditional 12/29/1983SE
K833941OrionIYE · Traditional 12/29/1983SE
K833846Process 100 STIZO · Traditional 12/16/1983SE
K837465Alcyon Rotational Cobalt Therapy · Traditional 06/28/1983SE
K837412Saturne I Linear Accelerator · Traditional 06/28/1983SE
K837336Verasun Radiation Therapy Simulation System · Traditional 04/29/1983SE

Questions and answers

When was Suspension 7 cleared by the FDA?

Suspension 7 (K843985) received a 510(k) decision of Substantially Equivalent on November 5, 1984, 25 days after the submission was received.