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FDA 510(k)

TeleScan

K-Number: K220767 · 2022-04-14

ApplicantBb Imaging
Decision Date2022-04-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TeleScan is a medical device manufactured by Bb Imaging. It received FDA 510(k) clearance on 2022-04-14 under approval number K220767. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TeleScan?

TeleScan is a medical device that received FDA 510(k) clearance on 2022-04-14. It is manufactured by Bb Imaging. The 510(k) number is K220767.

When was TeleScan approved by the FDA?

TeleScan received FDA 510(k) clearance on 2022-04-14, under approval number K220767.

What company makes TeleScan?

TeleScan is manufactured by Bb Imaging.

What is the FDA product code for TeleScan?

The FDA product code for TeleScan is LLZ.

Other Devices by Bb Imaging

K233634TeleScan

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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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