Angio Sys Fluoroscope Drape

FDA 510(k) K843259 · Angiosystems, Inc.

Substantially Equivalent

510(k) numberK843259

Submission

Device name
Angio Sys Fluoroscope Drape
Applicant
Angiosystems, Inc.
Mchenry, IL, US
Received
August 20, 1984
Decision date
September 21, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Angiosystems, Inc.

510(k)DeviceDecision
K905464Medical Procedure Kits/Arterial Blood SamplingCBT · Traditional 05/31/1991SEKD
K905459Surgical Procedure Tray/Laparoscopy CholecystectomLRO · Traditional 04/05/1991SE
K905461Procedure Kit/Routine Dental ProceduresEKS · Traditional 03/05/1991SEKD
K905466Sterile Disposable Surgical Drape/Abdominal DrapeKKX · Traditional 02/11/1991SE
K905465Sterile Dispos Surgical Drape/C-Section DrapeKKX · Traditional 02/11/1991SE
K905462Procedure Tray/For Various Ophthalmic ProceduresLRP · Traditional 02/06/1991SE
K905460Sterile Disposable Drape/Ophthalmic SurgeryHMT · Traditional 02/06/1991SE
K905463General Medical Procedure Kit/Skin PreparationFOZ · Traditional 01/22/1991SEKD
K864688Arnold-King Pressure DressingNAD · Traditional 01/12/1987SE
K843260Angiosys Femoral Angiography DrapeKKX · Traditional 09/21/1984SE

Questions and answers

When was Angio Sys Fluoroscope Drape cleared by the FDA?

Angio Sys Fluoroscope Drape (K843259) received a 510(k) decision of Substantially Equivalent on September 21, 1984, 32 days after the submission was received.