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FDA 510(k)

MULTITREAT 48

K-Number: K834308 · 1984-01-10

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date1984-01-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTITREAT 48 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 1984-01-10 under 510(k) number K834308. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTITREAT 48?

MULTITREAT 48 is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K834308.

When did MULTITREAT 48 receive FDA 510(k) clearance?

MULTITREAT 48 received FDA 510(k) clearance on 1984-01-10, under 510(k) number K834308.

Who is the listed applicant for MULTITREAT 48?

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 MULTITREAT 48?

The FDA product code for MULTITREAT 48 is JAQ.

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Other records listing Mick Radio-Nuclear Instruments, Inc. as applicant

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Related Devices (Code: JAQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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