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FDA 510(k)

K3 COMPUTER SYSTEMS

K-Number: K902977 · 1992-04-28

ApplicantDonald L. King M.D.
Decision Date1992-04-28
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

K3 COMPUTER SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Donald L. King M.D.. It received FDA 510(k) clearance on 1992-04-28 under 510(k) number K902977. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K3 COMPUTER SYSTEMS?

K3 COMPUTER SYSTEMS is a medical device that received FDA 510(k) clearance on 1992-04-28. The listed applicant is Donald L. King M.D.. The 510(k) number is K902977.

When did K3 COMPUTER SYSTEMS receive FDA 510(k) clearance?

K3 COMPUTER SYSTEMS received FDA 510(k) clearance on 1992-04-28, under 510(k) number K902977.

Who is the listed applicant for K3 COMPUTER SYSTEMS?

The FDA 510(k) record lists Donald L. King M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K3 COMPUTER SYSTEMS?

The FDA product code for K3 COMPUTER SYSTEMS is DPT.

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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Related Devices (Code: DPT)

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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