TBA
K-Number: K121269 · 2013-01-22
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Device Summary
Frequently Asked Questions
What is the TBA?
TBA is a medical device that received FDA 510(k) clearance on 2013-01-22. The listed applicant is Migada Plant. The 510(k) number is K121269.
When did TBA receive FDA 510(k) clearance?
TBA received FDA 510(k) clearance on 2013-01-22, under 510(k) number K121269.
Who is the listed applicant for TBA?
The FDA 510(k) record lists Migada Plant as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TBA?
The FDA product code for TBA is FPA.
Other records listing Migada Plant 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: FPA)
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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