Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NANMA ADJUSTABLE CONSTRICTION RING

K-Number: K013051 · 2002-08-22

ApplicantNanma Mfg Co., Ltd.
Decision Date2002-08-22
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NANMA ADJUSTABLE CONSTRICTION RING is the device name listed in this FDA 510(k) record. The listed applicant is Nanma Mfg Co., Ltd.. It received FDA 510(k) clearance on 2002-08-22 under 510(k) number K013051. 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 NANMA ADJUSTABLE CONSTRICTION RING?

NANMA ADJUSTABLE CONSTRICTION RING is a medical device that received FDA 510(k) clearance on 2002-08-22. The listed applicant is Nanma Mfg Co., Ltd.. The 510(k) number is K013051.

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

NANMA ADJUSTABLE CONSTRICTION RING received FDA 510(k) clearance on 2002-08-22, under 510(k) number K013051.

Who is the listed applicant for NANMA ADJUSTABLE CONSTRICTION RING?

The FDA 510(k) record lists Nanma Mfg Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NANMA ADJUSTABLE CONSTRICTION RING?

The FDA product code for NANMA ADJUSTABLE 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 Nanma Mfg Co., Ltd. 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.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SK030119NANMA ADJUSTABLE CONSTRICTION RINGK030913NANMA VACUUM PUMPK013113MODIFICATION TO NANMA VACUUM PUMPK013053MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RINGK993909NANMA VACUUM PUMP

View all 9 devices →

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.K020969VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , 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.

↑