BANANA RIBBED
K-Number: K063401 · 2007-03-26
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Device Summary
Frequently Asked Questions
What is the BANANA RIBBED?
BANANA RIBBED is a medical device that received FDA 510(k) clearance on 2007-03-26. The listed applicant is Medtech Products , Ltd.. The 510(k) number is K063401.
When did BANANA RIBBED receive FDA 510(k) clearance?
BANANA RIBBED received FDA 510(k) clearance on 2007-03-26, under 510(k) number K063401.
Who is the listed applicant for BANANA RIBBED?
The FDA 510(k) record lists Medtech Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BANANA RIBBED?
The FDA product code for BANANA RIBBED is HIS.
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 Medtech Products , Ltd. 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: HIS)
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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