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FDA 510(k)

SCAN300FP / RETROPAN (VDC)

K-Number: K051664 · 2005-07-20

ApplicantOy Ajat, Ltd.
Decision Date2005-07-20
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCAN300FP / RETROPAN (VDC) is the device name listed in this FDA 510(k) record. The listed applicant is Oy Ajat, Ltd.. It received FDA 510(k) clearance on 2005-07-20 under 510(k) number K051664. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCAN300FP / RETROPAN (VDC)?

SCAN300FP / RETROPAN (VDC) is a medical device that received FDA 510(k) clearance on 2005-07-20. The listed applicant is Oy Ajat, Ltd.. The 510(k) number is K051664.

When did SCAN300FP / RETROPAN (VDC) receive FDA 510(k) clearance?

SCAN300FP / RETROPAN (VDC) received FDA 510(k) clearance on 2005-07-20, under 510(k) number K051664.

Who is the listed applicant for SCAN300FP / RETROPAN (VDC)?

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

What is the FDA product code for SCAN300FP / RETROPAN (VDC)?

The FDA product code for SCAN300FP / RETROPAN (VDC) is MUH.

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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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