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FDA 510(k)

WILLI GELLER CREATION II PORCELAIN

K-Number: K043468 · 2005-01-12

ApplicantJensen Int'L, Inc.
Decision Date2005-01-12
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILLI GELLER CREATION II PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Jensen Int'L, Inc.. It received FDA 510(k) clearance on 2005-01-12 under 510(k) number K043468. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLI GELLER CREATION II PORCELAIN?

WILLI GELLER CREATION II PORCELAIN is a medical device that received FDA 510(k) clearance on 2005-01-12. The listed applicant is Jensen Int'L, Inc.. The 510(k) number is K043468.

When did WILLI GELLER CREATION II PORCELAIN receive FDA 510(k) clearance?

WILLI GELLER CREATION II PORCELAIN received FDA 510(k) clearance on 2005-01-12, under 510(k) number K043468.

Who is the listed applicant for WILLI GELLER CREATION II PORCELAIN?

The FDA 510(k) record lists Jensen Int'L, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILLI GELLER CREATION II PORCELAIN?

The FDA product code for WILLI GELLER CREATION II PORCELAIN is EIH.

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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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