Cement Extraction Instrumentation

FDA 510(k) K822554 · Surgi-Quip Inc.U

Substantially Equivalent

510(k) numberK822554

Submission

Device name
Cement Extraction Instrumentation
Applicant
Surgi-Quip Inc.U
Mchenry, IL, US
Received
August 24, 1982
Decision date
September 14, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Surgi-Quip Inc.U

510(k)DeviceDecision
K841116Mobile Ophthalmic Operating TableFWX · Traditional 05/09/1984SE
K841115Charles/Mcintyre Giant Break TableFQO · Traditional 05/09/1984SE
K840004Wee Bag O'MercuryLCC · Traditional 03/22/1984SE
K832887Electronic UnitEPT · Traditional 10/04/1983SE
K822427Self-Contained Mobile Ophthal. Oper. .FSE · Traditional 09/14/1982SE
K822428Surgi-Quip Microscope StandHBN · Traditional 09/02/1982SE
K822426Mcintyre Microscope StandHBN · Traditional 09/02/1982SE

Questions and answers

When was Cement Extraction Instrumentation cleared by the FDA?

Cement Extraction Instrumentation (K822554) received a 510(k) decision of Substantially Equivalent on September 14, 1982, 21 days after the submission was received.