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FDA 510(k)

QRI-FLOW URINE FLOW MEASURING DEVICE

K-Number: K851266 · 1985-06-27

ApplicantBio-Flow, Inc.
Decision Date1985-06-27
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QRI-FLOW URINE FLOW MEASURING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Flow, Inc.. It received FDA 510(k) clearance on 1985-06-27 under 510(k) number K851266. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QRI-FLOW URINE FLOW MEASURING DEVICE?

QRI-FLOW URINE FLOW MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1985-06-27. The listed applicant is Bio-Flow, Inc.. The 510(k) number is K851266.

When did QRI-FLOW URINE FLOW MEASURING DEVICE receive FDA 510(k) clearance?

QRI-FLOW URINE FLOW MEASURING DEVICE received FDA 510(k) clearance on 1985-06-27, under 510(k) number K851266.

Who is the listed applicant for QRI-FLOW URINE FLOW MEASURING DEVICE?

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

What is the FDA product code for QRI-FLOW URINE FLOW MEASURING DEVICE?

The FDA product code for QRI-FLOW URINE FLOW MEASURING DEVICE is KNX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Bio-Flow, 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.

K862251MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE

Related Devices (Code: KNX)

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.

K110518IBAGFuture Path Medical, LLCK9733644L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAGMaersk Medical A/SK972887MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAGMedline Industries, Inc.K971271BESECURE EXTERNAL URINARY COLLECTION SYSTEMUrology Research Intl., Inc.K971929AMSINO URINARY LEG BAGAmsino Intl., Inc.K971764WELCON HUE-VU URINARY DRAINAGE BAGWelcon, Inc.

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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