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FDA 510(k)

ISOCENTRIC BEAM CHECKER

K-Number: K993959 · 2000-02-14

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date2000-02-14
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ISOCENTRIC BEAM CHECKER is the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 2000-02-14 under 510(k) number K993959. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOCENTRIC BEAM CHECKER?

ISOCENTRIC BEAM CHECKER is a medical device that received FDA 510(k) clearance on 2000-02-14. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K993959.

When did ISOCENTRIC BEAM CHECKER receive FDA 510(k) clearance?

ISOCENTRIC BEAM CHECKER received FDA 510(k) clearance on 2000-02-14, under 510(k) number K993959.

Who is the listed applicant for ISOCENTRIC BEAM CHECKER?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ISOCENTRIC BEAM CHECKER?

The FDA product code for ISOCENTRIC BEAM CHECKER is IYE.

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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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