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FDA 510(k)

WILLI GELLER CERAMIC CREATION & SURPRISE

K-Number: K900209 · 1990-04-09

ApplicantCreation North America, Inc.
Decision Date1990-04-09
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILLI GELLER CERAMIC CREATION & SURPRISE is the device name listed in this FDA 510(k) record. The listed applicant is Creation North America, Inc.. It received FDA 510(k) clearance on 1990-04-09 under 510(k) number K900209. 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 CERAMIC CREATION & SURPRISE?

WILLI GELLER CERAMIC CREATION & SURPRISE is a medical device that received FDA 510(k) clearance on 1990-04-09. The listed applicant is Creation North America, Inc.. The 510(k) number is K900209.

When did WILLI GELLER CERAMIC CREATION & SURPRISE receive FDA 510(k) clearance?

WILLI GELLER CERAMIC CREATION & SURPRISE received FDA 510(k) clearance on 1990-04-09, under 510(k) number K900209.

Who is the listed applicant for WILLI GELLER CERAMIC CREATION & SURPRISE?

The FDA 510(k) record lists Creation North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILLI GELLER CERAMIC CREATION & SURPRISE?

The FDA product code for WILLI GELLER CERAMIC CREATION & SURPRISE is EIH.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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