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FDA 510(k)

CIVCO/SUPER SCAN

K-Number: K841332 · 1984-05-09

ApplicantCIVCO Medical Instruments Co., Inc.
Decision Date1984-05-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CIVCO/SUPER SCAN is the device name listed in this FDA 510(k) record. The listed applicant is CIVCO Medical Instruments Co., Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841332. 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 CIVCO/SUPER SCAN?

CIVCO/SUPER SCAN is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K841332.

When did CIVCO/SUPER SCAN receive FDA 510(k) clearance?

CIVCO/SUPER SCAN received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841332.

Who is the listed applicant for CIVCO/SUPER SCAN?

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

What is the FDA product code for CIVCO/SUPER SCAN?

The FDA product code for CIVCO/SUPER SCAN 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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