UR 150-UR 150T— 510(k) K801723

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K801723 for UR 150-UR 150T, Substantially Equivalent on 1980-08-13. Applicant: Siemens Corp.. Device class: 1.

Clearance details

Applicant: Siemens Corp.
Product code: Code KQS
Device class: Class 1
Regulation: 21 CFR 876.4890
Advisory panel: Gastroenterology, Urology
Date received: 1980-07-24
Decision date: 1980-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQS

K955019 — UROTRACT I1995-12-06
K872022 — UROVIEW1987-07-16
K864846 — RADIOGRAPHIC - LEG SECTION1986-12-24
K860040 — HYDRAJUST III UROLOGICAL TABLE1986-02-10
K852127 — AMSCO URO-ENDO MOBILE TABLE1985-08-08

More clearances from Siemens Corp.

K103360 — DIMENSION VISTA DIGITOXIN CALIBRATOR - DGTX CAL2010-12-17
K993947 — KOORDINANT ANGIOGRAPHIC AND OPERATING ROOM MODEL X-RAY TABLE FAMILY1999-12-21
K992925 — AX WORKSTATION DR-VIEWER SOFTWARE OPTION1999-11-23
K991652 — HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM1999-08-03
K991600 — SOMATOM PLUS 4 WITH SLIDING GANTRY OPTION1999-06-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.