MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING
K-Number: K013053 · 2002-05-09
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Device Summary
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.
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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