Z XT Radiation Therapy Treatment Table

FDA 510(k) K910971 · Siemens Medical Laboratories, Inc.

Substantially Equivalent

510(k) numberK910971

Submission

Device name
Z XT Radiation Therapy Treatment Table
Applicant
Siemens Medical Laboratories, Inc.
Concord, CA, US
Received
March 7, 1991
Decision date
May 3, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JAI – Couch, Radiation Therapy, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 892.5770
Specialty
Radiology

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Questions and answers

When was Z XT Radiation Therapy Treatment Table cleared by the FDA?

Z XT Radiation Therapy Treatment Table (K910971) received a 510(k) decision of Substantially Equivalent on May 3, 1991, 57 days after the submission was received.

What is the product code of K910971?

The FDA product code is JAI – Couch, Radiation Therapy, Powered, a Class II (moderate risk) device regulated under 21 CFR 892.5770.