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)

MENICON SF-P

K-Number: K000233 · 2000-05-19

Decision Date2000-05-19
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENICON SF-P is the device name listed in this FDA 510(k) record. The listed applicant is Menicon Co, Ltd.. It received FDA 510(k) clearance on 2000-05-19 under 510(k) number K000233. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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.

↑