Uroskop a and B

FDA 510(k) K781532 · Siemens Corp.

Substantially Equivalent

510(k) numberK781532

Submission

Device name
Uroskop a and B
Applicant
Siemens Corp.
Mchenry, IL, US
Received
September 6, 1978
Decision date
September 14, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IXR – Table, Radiographic, Tilting
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1980
Specialty
Radiology

Other 510(k)s with product code IXR

510(k)DeviceApplicantDecision
K000412Vision R/F Tilting TableIXR · Traditional Villa Sistemi Medicali S.P.A.04/24/2000SE
K973039Legacy/Legacy-D TableIXR · Traditional GE Medical Systems10/16/1997SE
K971128CAP-35B Iii/Cine 275IXR · Traditional Jamieson Film Co.04/28/1997SE
K970640Philips Easy DiagnostIXR · Traditional Philips Medical Systems North America, Inc.03/21/1997SE
K965105Electrophysiology Tilt Table Model #9660IXR · Traditional U.S. Imaging Tables, Inc.01/30/1997SE
K965096Fluoroview Series Fluoroscopic TablesIXR · Traditional U.S. Imaging Tables, Inc.01/27/1997SE
K963851Tilting Radiographic Table (Remote)IXR · Traditional Acoma Medical Imaging, Inc.01/23/1997SE
K961022Tangent Vi TableIXR · Traditional Fischer Imaging Corp.05/03/1996SE
K954356Compax 90/15EIXR · Traditional General Electric Co.10/07/1995SE
K953557Surgical C-Arm Table, 9610IXR · Traditional U.S. Imaging Tables, Inc.09/26/1995SE

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Questions and answers

When was Uroskop a and B cleared by the FDA?

Uroskop a and B (K781532) received a 510(k) decision of Substantially Equivalent on September 14, 1978, 8 days after the submission was received.

What is the product code of K781532?

The FDA product code is IXR – Table, Radiographic, Tilting, a Class II (moderate risk) device regulated under 21 CFR 892.1980.