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FDA 510(k)

VELCRO FISTULA PRESSURE CLAMPS

K-Number: K853536 · 1985-10-17

ApplicantCp Medical
Decision Date1985-10-17
Product CodeKXM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VELCRO FISTULA PRESSURE CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Cp Medical. It received FDA 510(k) clearance on 1985-10-17 under 510(k) number K853536. The device is classified under product code KXM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VELCRO FISTULA PRESSURE CLAMPS?

VELCRO FISTULA PRESSURE CLAMPS is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Cp Medical. The 510(k) number is K853536.

When did VELCRO FISTULA PRESSURE CLAMPS receive FDA 510(k) clearance?

VELCRO FISTULA PRESSURE CLAMPS received FDA 510(k) clearance on 1985-10-17, under 510(k) number K853536.

Who is the listed applicant for VELCRO FISTULA PRESSURE CLAMPS?

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

What is the FDA product code for VELCRO FISTULA PRESSURE CLAMPS?

The FDA product code for VELCRO FISTULA PRESSURE CLAMPS is KXM.

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 Cp Medical 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.

K094028CP-FIBER (ORTHOFIBER)K072229MONOSWIFTK071550PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERSK060987OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31K041894ORTHOFIBERK034062CP SLEEVE AND RIVER SLEEVE

View all 31 devices →

Related Devices (Code: KXM)

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.

K925581BAXTER BIOSTAT 1000 UREA MONITORBaxter Healthcare CorpK863471COLORADO MEDICAL MODEL PTC 1000Colorado Medical, Inc.K831402PRESSURE MONITOR & CONTROL UNIT APC-02AParker Hannifin 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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