Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

UR 150-UR 150T

K-Number: K801723 · 1980-08-13

ApplicantSiemens Corp.
Decision Date1980-08-13
Product CodeKQS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UR 150-UR 150T is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801723. The device is classified under product code KQS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UR 150-UR 150T?

UR 150-UR 150T is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Siemens Corp.. The 510(k) number is K801723.

When did UR 150-UR 150T receive FDA 510(k) clearance?

UR 150-UR 150T received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801723.

Who is the listed applicant for UR 150-UR 150T?

The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UR 150-UR 150T?

The FDA product code for UR 150-UR 150T is KQS.

Other records listing Siemens Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K103360DIMENSION VISTA DIGITOXIN CALIBRATOR - DGTX CALK993947KOORDINANT ANGIOGRAPHIC AND OPERATING ROOM MODEL X-RAY TABLE FAMILYK992925AX WORKSTATION DR-VIEWER SOFTWARE OPTIONK991652HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEMK991600SOMATOM PLUS 4 WITH SLIDING GANTRY OPTIONK984221FUNCTIONAL MRI PACKAGE FOR MAGETETOM VISION MR

View all 66 devices →

Related Devices (Code: KQS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K955019UROTRACT IDornier Medtech America, Inc.K872022UROVIEWOec-Diasonics, Inc.K864846RADIOGRAPHIC - LEG SECTIONAmerican Sterilizer Co.K860040HYDRAJUST III UROLOGICAL TABLEMallinckrodt Group, Inc.K852127AMSCO URO-ENDO MOBILE TABLEAmerican Sterilizer Co.K791699HYDRADJUST II UROLOGICAL TABLESybron Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑