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FDA 510(k)

AROMATIC AND FLAVORED TONGUE DEPRESSOR

K-Number: K992995 · 1999-12-09

Decision Date1999-12-09
Product CodeFMA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AROMATIC AND FLAVORED TONGUE DEPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Aga Plastic Ind. Com. Ltda.. It received FDA 510(k) clearance on 1999-12-09 under 510(k) number K992995. The device is classified under product code FMA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AROMATIC AND FLAVORED TONGUE DEPRESSOR?

AROMATIC AND FLAVORED TONGUE DEPRESSOR is a medical device that received FDA 510(k) clearance on 1999-12-09. The listed applicant is Aga Plastic Ind. Com. Ltda.. The 510(k) number is K992995.

When did AROMATIC AND FLAVORED TONGUE DEPRESSOR receive FDA 510(k) clearance?

AROMATIC AND FLAVORED TONGUE DEPRESSOR received FDA 510(k) clearance on 1999-12-09, under 510(k) number K992995.

Who is the listed applicant for AROMATIC AND FLAVORED TONGUE DEPRESSOR?

The FDA 510(k) record lists Aga Plastic Ind. Com. Ltda. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AROMATIC AND FLAVORED TONGUE DEPRESSOR?

The FDA product code for AROMATIC AND FLAVORED TONGUE DEPRESSOR is FMA.

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 Aga Plastic Ind. Com. Ltda. 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: FMA)

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

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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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