BANTAM
K-Number: K091242 · 2009-07-06
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Device Summary
Frequently Asked Questions
What is the BANTAM?
BANTAM is a medical device that received FDA 510(k) clearance on 2009-07-06. The listed applicant is Altimate Medical, Inc.. The 510(k) number is K091242.
When did BANTAM receive FDA 510(k) clearance?
BANTAM received FDA 510(k) clearance on 2009-07-06, under 510(k) number K091242.
Who is the listed applicant for BANTAM?
The FDA 510(k) record lists Altimate Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BANTAM?
The FDA product code for BANTAM is INO.
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 Altimate Medical, 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: INO)
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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