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FDA 510(k)

MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE

K-Number: K862251 · 1986-09-04

ApplicantBio-Flow, Inc.
Decision Date1986-09-04
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED BIO-FLOW MODEL 200 URINE FLOW 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 1986-09-04 under 510(k) number K862251. 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 MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE?

MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE is a medical device that received FDA 510(k) clearance on 1986-09-04. The listed applicant is Bio-Flow, Inc.. The 510(k) number is K862251.

When did MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE receive FDA 510(k) clearance?

MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE received FDA 510(k) clearance on 1986-09-04, under 510(k) number K862251.

Who is the listed applicant for MODIFIED BIO-FLOW MODEL 200 URINE FLOW 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 MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE?

The FDA product code for MODIFIED BIO-FLOW MODEL 200 URINE FLOW 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.

K851266QRI-FLOW URINE FLOW MEASURING 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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