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FDA 510(k)

PERMA-DOC PHANTOM

K-Number: K993960 · 2000-02-14

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

Device Summary

PERMA-DOC PHANTOM 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 K993960. 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 PERMA-DOC PHANTOM?

PERMA-DOC PHANTOM 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 K993960.

When did PERMA-DOC PHANTOM receive FDA 510(k) clearance?

PERMA-DOC PHANTOM received FDA 510(k) clearance on 2000-02-14, under 510(k) number K993960.

Who is the listed applicant for PERMA-DOC PHANTOM?

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 PERMA-DOC PHANTOM?

The FDA product code for PERMA-DOC PHANTOM 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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