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FDA 510(k)

RADSCAN EQUIPMENT SLICKER

K-Number: K101350 · 2011-01-04

ApplicantRadscan Medical Equipment, Inc.
Decision Date2011-01-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RADSCAN EQUIPMENT SLICKER is the device name listed in this FDA 510(k) record. The listed applicant is Radscan Medical Equipment, Inc.. It received FDA 510(k) clearance on 2011-01-04 under 510(k) number K101350. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADSCAN EQUIPMENT SLICKER?

RADSCAN EQUIPMENT SLICKER is a medical device that received FDA 510(k) clearance on 2011-01-04. The listed applicant is Radscan Medical Equipment, Inc.. The 510(k) number is K101350.

When did RADSCAN EQUIPMENT SLICKER receive FDA 510(k) clearance?

RADSCAN EQUIPMENT SLICKER received FDA 510(k) clearance on 2011-01-04, under 510(k) number K101350.

Who is the listed applicant for RADSCAN EQUIPMENT SLICKER?

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

What is the FDA product code for RADSCAN EQUIPMENT SLICKER?

The FDA product code for RADSCAN EQUIPMENT SLICKER is KKX.

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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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