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FDA 510(k)

SILENT SCAN

K-Number: K921891 · 1993-05-13

ApplicantAvotec, Inc.
Decision Date1993-05-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SILENT SCAN is the device name listed in this FDA 510(k) record. The listed applicant is Avotec, Inc.. It received FDA 510(k) clearance on 1993-05-13 under 510(k) number K921891. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILENT SCAN?

SILENT SCAN is a medical device that received FDA 510(k) clearance on 1993-05-13. The listed applicant is Avotec, Inc.. The 510(k) number is K921891.

When did SILENT SCAN receive FDA 510(k) clearance?

SILENT SCAN received FDA 510(k) clearance on 1993-05-13, under 510(k) number K921891.

Who is the listed applicant for SILENT SCAN?

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

What is the FDA product code for SILENT SCAN?

The FDA product code for SILENT SCAN is LNH.

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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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