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FDA 510(k)

UROVIEW

K-Number: K872022 · 1987-07-16

ApplicantOec-Diasonics, Inc.
Decision Date1987-07-16
Product CodeKQS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UROVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Oec-Diasonics, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K872022. 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 UROVIEW?

UROVIEW is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Oec-Diasonics, Inc.. The 510(k) number is K872022.

When did UROVIEW receive FDA 510(k) clearance?

UROVIEW received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872022.

Who is the listed applicant for UROVIEW?

The FDA 510(k) record lists Oec-Diasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UROVIEW?

The FDA product code for UROVIEW is KQS.

Related Clinical Trials

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.

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Other records listing Oec-Diasonics, Inc. 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.

K9260569600 FLUOROSCOPIC IMAGING SYSTEMK924879EP 3000K914446UROVIEW 2000, MODIFICATIONK896583F.A.S.T. TABLEK893475UROVIEW IIK864837MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM

View all 8 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.K864846RADIOGRAPHIC - LEG SECTIONAmerican Sterilizer Co.K860040HYDRAJUST III UROLOGICAL TABLEMallinckrodt Group, Inc.K852127AMSCO URO-ENDO MOBILE TABLEAmerican Sterilizer Co.K801723UR 150-UR 150TSiemens Corp.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.

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