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FDA 510(k)

RELIANT CONSTRICTION RING

K-Number: K940995 · 1994-06-14

ApplicantWalling Medical Equipment Co.
Decision Date1994-06-14
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RELIANT CONSTRICTION RING is the device name listed in this FDA 510(k) record. The listed applicant is Walling Medical Equipment Co.. It received FDA 510(k) clearance on 1994-06-14 under 510(k) number K940995. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANT CONSTRICTION RING?

RELIANT CONSTRICTION RING is a medical device that received FDA 510(k) clearance on 1994-06-14. The listed applicant is Walling Medical Equipment Co.. The 510(k) number is K940995.

When did RELIANT CONSTRICTION RING receive FDA 510(k) clearance?

RELIANT CONSTRICTION RING received FDA 510(k) clearance on 1994-06-14, under 510(k) number K940995.

Who is the listed applicant for RELIANT CONSTRICTION RING?

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

What is the FDA product code for RELIANT CONSTRICTION RING?

The FDA product code for RELIANT CONSTRICTION RING is LKY.

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 Walling Medical Equipment Co. 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.

K980567CHARGER (ED)K980752XTENDK971768RELIANT CHARGER

Related Devices (Code: LKY)

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.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SNanma Mfg Co., Ltd.K032776VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , Ltd.K030119NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.K030913NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013113MODIFICATION TO NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013051NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.

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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