Imaging Table

FDA 510(k) K951146 · Septa Corp.

Substantially Equivalent

510(k) numberK951146

Submission

Device name
Imaging Table
Applicant
Septa Corp.
Mason, NH, US
Received
March 13, 1995
Decision date
May 4, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KXJ – Table, Radiologic
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1980
Specialty
Radiology

Other 510(k)s with product code KXJ

510(k)DeviceApplicantDecision
K050190ApolloKXJ · Abbreviated Villa Sistemi Medicali S.P.A.03/25/2005SE
K963905Radiographic Itt TableKXJ · Traditional X-Ray Technologies, Inc.11/12/1996SE
K955414XRT 400KXJ · Traditional Wuestec Medical, Inc.07/24/1996SE
K950068Carbon Fiber Couch InsertKXJ · Traditional Medtec, Inc.04/06/1995SE
K950442Infrared Exposure Hand SwitchKXJ · Traditional Medical X-Ray Intl., Inc.03/31/1995SE
K940696Syncra Tilt Option for Angio Diagnost 5KXJ · Traditional Philips Medical Systems North America, Inc.03/16/1994SE
K931724Electrophysiology (Ep) Table Ep 2000 SeriesKXJ · Traditional Continental X-Ray Corp.06/14/1993SE
K926407Model Cole TAB-2 Table W/Model Cole SFD-2 SpotfilmKXJ · Traditional Nucletron-Oldelft Corp.03/31/1993SE
K922098CAG-02AKXJ · Traditional Toshiba America Medical Systems, In.C07/27/1992SE
K913121Omniflex Overhead Tubecrane CAT.#S-9108/#6713.400KXJ · Traditional Continental X-Ray Corp.08/16/1991SE

Questions and answers

When was Imaging Table cleared by the FDA?

Imaging Table (K951146) received a 510(k) decision of Substantially Equivalent on May 4, 1995, 52 days after the submission was received.

What is the product code of K951146?

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