FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES
K-Number: K964317 · 1997-01-24
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Device Summary
Frequently Asked Questions
What is the FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES?
FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES is a medical device that received FDA 510(k) clearance on 1997-01-24. The listed applicant is Nantong Ruchang Latex Products Co., Ltd.. The 510(k) number is K964317.
When did FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES receive FDA 510(k) clearance?
FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES received FDA 510(k) clearance on 1997-01-24, under 510(k) number K964317.
Who is the listed applicant for FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES?
The FDA 510(k) record lists Nantong Ruchang Latex Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES?
The FDA product code for FOXELL, MEDIGUARD, PLUS MULTIPLE BRAND NAMES is LYY.
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 Nantong Ruchang Latex Products 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: LYY)
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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