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FDA 510(k)

GAMMA MED II

K-Number: K781274 · 1978-08-10

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date1978-08-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GAMMA MED II 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 1978-08-10 under 510(k) number K781274. 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 GAMMA MED II?

GAMMA MED II is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K781274.

When did GAMMA MED II receive FDA 510(k) clearance?

GAMMA MED II received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781274.

Who is the listed applicant for GAMMA MED II?

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 GAMMA MED II?

The FDA product code for GAMMA MED II is JAQ.

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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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