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FDA 510(k)

BABY TEETHER, MODEL 20104

K-Number: K014023 · 2002-08-02

ApplicantAngelina Trading, Inc.
Decision Date2002-08-02
Product CodeKKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BABY TEETHER, MODEL 20104 is the device name listed in this FDA 510(k) record. The listed applicant is Angelina Trading, Inc.. It received FDA 510(k) clearance on 2002-08-02 under 510(k) number K014023. The device is classified under product code KKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BABY TEETHER, MODEL 20104?

BABY TEETHER, MODEL 20104 is a medical device that received FDA 510(k) clearance on 2002-08-02. The listed applicant is Angelina Trading, Inc.. The 510(k) number is K014023.

When did BABY TEETHER, MODEL 20104 receive FDA 510(k) clearance?

BABY TEETHER, MODEL 20104 received FDA 510(k) clearance on 2002-08-02, under 510(k) number K014023.

Who is the listed applicant for BABY TEETHER, MODEL 20104?

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

What is the FDA product code for BABY TEETHER, MODEL 20104?

The FDA product code for BABY TEETHER, MODEL 20104 is KKO.

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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.

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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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