WILLI GELLER CREATION ZI PORCELAIN
K-Number: K043201 · 2005-01-11
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Device Summary
Frequently Asked Questions
What is the WILLI GELLER CREATION ZI PORCELAIN?
WILLI GELLER CREATION ZI PORCELAIN is a medical device that received FDA 510(k) clearance on 2005-01-11. The listed applicant is Jensen Industries, Inc.. The 510(k) number is K043201.
When did WILLI GELLER CREATION ZI PORCELAIN receive FDA 510(k) clearance?
WILLI GELLER CREATION ZI PORCELAIN received FDA 510(k) clearance on 2005-01-11, under 510(k) number K043201.
Who is the listed applicant for WILLI GELLER CREATION ZI PORCELAIN?
The FDA 510(k) record lists Jensen Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WILLI GELLER CREATION ZI PORCELAIN?
The FDA product code for WILLI GELLER CREATION ZI PORCELAIN 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 Jensen Industries, 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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