NORITAKE SUPER PORCELAIN EX-3
K-Number: K884356 · 1989-01-10
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Device Summary
Frequently Asked Questions
What is the NORITAKE SUPER PORCELAIN EX-3?
NORITAKE SUPER PORCELAIN EX-3 is a medical device that received FDA 510(k) clearance on 1989-01-10. The listed applicant is Noritake Co., Inc.. The 510(k) number is K884356.
When did NORITAKE SUPER PORCELAIN EX-3 receive FDA 510(k) clearance?
NORITAKE SUPER PORCELAIN EX-3 received FDA 510(k) clearance on 1989-01-10, under 510(k) number K884356.
Who is the listed applicant for NORITAKE SUPER PORCELAIN EX-3?
The FDA 510(k) record lists Noritake Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NORITAKE SUPER PORCELAIN EX-3?
The FDA product code for NORITAKE SUPER PORCELAIN EX-3 is EIH.
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 Noritake Co., Inc. 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: EIH)
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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