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FDA 510(k)

DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM

K-Number: K837100 · 1983-03-24

ApplicantDr. John D. Reid B.A., D.C.
Decision Date1983-03-24
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM is the device name listed in this FDA 510(k) record. The listed applicant is Dr. John D. Reid B.A., D.C.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K837100. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM?

DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Dr. John D. Reid B.A., D.C.. The 510(k) number is K837100.

When did DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM receive FDA 510(k) clearance?

DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM received FDA 510(k) clearance on 1983-03-24, under 510(k) number K837100.

Who is the listed applicant for DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM?

The FDA 510(k) record lists Dr. John D. Reid B.A., D.C. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Dr. John D. Reid B.A., D.C. as applicant

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.

K821524CHIROPRATIC INFRA-RED CRYSTAL PAK

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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