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FDA 510(k)

MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING

K-Number: K013053 · 2002-05-09

Decision Date2002-05-09
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO NANMA NON-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 2002-05-09 under 510(k) number K013053. 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 MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING?

MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING is a medical device that received FDA 510(k) clearance on 2002-05-09. The listed applicant is Nanma Mfg Co., Ltd.. The 510(k) number is K013053.

When did MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING receive FDA 510(k) clearance?

MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING received FDA 510(k) clearance on 2002-05-09, under 510(k) number K013053.

Who is the listed applicant for MODIFICATION TO NANMA NON-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 MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING?

The FDA product code for MODIFICATION TO NANMA NON-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.

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.

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.

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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