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FDA 510(k)

VITASCAN LT SCANMASTER

K-Number: K121689 · 2012-09-19

ApplicantVitacon Medical, Inc.
Decision Date2012-09-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VITASCAN LT SCANMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Vitacon Medical, Inc.. It received FDA 510(k) clearance on 2012-09-19 under 510(k) number K121689. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITASCAN LT SCANMASTER?

VITASCAN LT SCANMASTER is a medical device that received FDA 510(k) clearance on 2012-09-19. The listed applicant is Vitacon Medical, Inc.. The 510(k) number is K121689.

When did VITASCAN LT SCANMASTER receive FDA 510(k) clearance?

VITASCAN LT SCANMASTER received FDA 510(k) clearance on 2012-09-19, under 510(k) number K121689.

Who is the listed applicant for VITASCAN LT SCANMASTER?

The FDA 510(k) record lists Vitacon Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITASCAN LT SCANMASTER?

The FDA product code for VITASCAN LT SCANMASTER is IYO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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