FDA 510(k)

META III

K-Number: K790300 · 1979-03-27

Decision Date1979-03-27

Product CodeDPS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

META III is the device name listed in this FDA 510(k) record. The listed applicant is Hittman Medical Systems. It received FDA 510(k) clearance on 1979-03-27 under 510(k) number K790300. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the META III?

META III is a medical device that received FDA 510(k) clearance on 1979-03-27. The listed applicant is Hittman Medical Systems. The 510(k) number is K790300.

When did META III receive FDA 510(k) clearance?

META III received FDA 510(k) clearance on 1979-03-27, under 510(k) number K790300.

Who is the listed applicant for META III?

The FDA 510(k) record lists Hittman Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for META III?

The FDA product code for META III is DPS.

Other records listing Hittman Medical Systems 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.

K832772SATURN-24HR. HOLTER SCANNER K791632COMPU-SCAN

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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.