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FDA 510(k)

MM-22 MICROTRON

K-Number: K827704 · 1982-10-07

ApplicantInstrument AB Scanditronix
Decision Date1982-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

MM-22 MICROTRON is the device name listed in this FDA 510(k) record. The listed applicant is Instrument AB Scanditronix. It received FDA 510(k) clearance on 1982-10-07 under 510(k) number K827704. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MM-22 MICROTRON?

MM-22 MICROTRON is a medical device that received FDA 510(k) clearance on 1982-10-07. The listed applicant is Instrument AB Scanditronix. The 510(k) number is K827704.

When did MM-22 MICROTRON receive FDA 510(k) clearance?

MM-22 MICROTRON received FDA 510(k) clearance on 1982-10-07, under 510(k) number K827704.

Who is the listed applicant for MM-22 MICROTRON?

The FDA 510(k) record lists Instrument AB Scanditronix as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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

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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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