Argon Laser Surgical System 770

FDA 510(k) K833387 · Cooper Medical Corp.

Substantially Equivalent

510(k) numberK833387

Submission

Device name
Argon Laser Surgical System 770
Applicant
Cooper Medical Corp.
Mchenry, IL, US
Received
September 29, 1983
Decision date
April 18, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Cooper Medical Corp.

510(k)DeviceDecision
K840144Yag Laser 8000 Gastrointestinal BleeFCG · Traditional 05/18/1984SE
K833497Cooper Medical Model 770LLF · Traditional 04/17/1984SE
K832703Argon Laser Sys-Model 5000HQE · Traditional 01/30/1984SE
K820261Monitor CO2 Laser SystemHHR · Traditional 03/05/1982SE

Questions and answers

When was Argon Laser Surgical System 770 cleared by the FDA?

Argon Laser Surgical System 770 (K833387) received a 510(k) decision of Substantially Equivalent on April 18, 1984, 202 days after the submission was received.