MENICON SF-P
K-Number: K000233 · 2000-05-19
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Device Summary
Frequently Asked Questions
What is the MENICON SF-P?
MENICON SF-P is a medical device that received FDA 510(k) clearance on 2000-05-19. The listed applicant is Menicon Co, Ltd.. The 510(k) number is K000233.
When did MENICON SF-P receive FDA 510(k) clearance?
MENICON SF-P received FDA 510(k) clearance on 2000-05-19, under 510(k) number K000233.
Who is the listed applicant for MENICON SF-P?
The FDA 510(k) record lists Menicon Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MENICON SF-P?
The FDA product code for MENICON SF-P is HQD.
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 Menicon 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: HQD)
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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