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FDA 510(k)

BANTAM,48XXXXXX, 50XXXXXX

K-Number: K093139 · 2009-12-30

ApplicantClearStream Technologies , Ltd.
Decision Date2009-12-30
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BANTAM,48XXXXXX, 50XXXXXX is the device name listed in this FDA 510(k) record. The listed applicant is ClearStream Technologies , Ltd.. It received FDA 510(k) clearance on 2009-12-30 under 510(k) number K093139. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANTAM,48XXXXXX, 50XXXXXX?

BANTAM,48XXXXXX, 50XXXXXX is a medical device that received FDA 510(k) clearance on 2009-12-30. The listed applicant is ClearStream Technologies , Ltd.. The 510(k) number is K093139.

When did BANTAM,48XXXXXX, 50XXXXXX receive FDA 510(k) clearance?

BANTAM,48XXXXXX, 50XXXXXX received FDA 510(k) clearance on 2009-12-30, under 510(k) number K093139.

Who is the listed applicant for BANTAM,48XXXXXX, 50XXXXXX?

The FDA 510(k) record lists ClearStream Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BANTAM,48XXXXXX, 50XXXXXX?

The FDA product code for BANTAM,48XXXXXX, 50XXXXXX is LIT.

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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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