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FDA 510(k)

SCANNER-SV

K-Number: K782158 · 1979-01-25

ApplicantHrl, Inc.
Decision Date1979-01-25
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCANNER-SV is the device name listed in this FDA 510(k) record. The listed applicant is Hrl, Inc.. It received FDA 510(k) clearance on 1979-01-25 under 510(k) number K782158. 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 SCANNER-SV?

SCANNER-SV is a medical device that received FDA 510(k) clearance on 1979-01-25. The listed applicant is Hrl, Inc.. The 510(k) number is K782158.

When did SCANNER-SV receive FDA 510(k) clearance?

SCANNER-SV received FDA 510(k) clearance on 1979-01-25, under 510(k) number K782158.

Who is the listed applicant for SCANNER-SV?

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

What is the FDA product code for SCANNER-SV?

The FDA product code for SCANNER-SV is IYO.

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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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