BERRY FRUITY TEETHER
K-Number: K053493 · 2006-02-22
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Device Summary
Frequently Asked Questions
What is the BERRY FRUITY TEETHER?
BERRY FRUITY TEETHER is a medical device that received FDA 510(k) clearance on 2006-02-22. The listed applicant is Evenflo Company, Inc.. The 510(k) number is K053493.
When did BERRY FRUITY TEETHER receive FDA 510(k) clearance?
BERRY FRUITY TEETHER received FDA 510(k) clearance on 2006-02-22, under 510(k) number K053493.
Who is the listed applicant for BERRY FRUITY TEETHER?
The FDA 510(k) record lists Evenflo Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BERRY FRUITY TEETHER?
The FDA product code for BERRY FRUITY TEETHER is KKO.
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 Evenflo Company, 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: KKO)
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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