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FDA 510(k)

VITA-STAT MODEL 9000-S

K-Number: K811148 · 1981-06-30

ApplicantViat-Stat
Decision Date1981-06-30
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITA-STAT MODEL 9000-S is the device name listed in this FDA 510(k) record. The listed applicant is Viat-Stat. It received FDA 510(k) clearance on 1981-06-30 under 510(k) number K811148. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA-STAT MODEL 9000-S?

VITA-STAT MODEL 9000-S is a medical device that received FDA 510(k) clearance on 1981-06-30. The listed applicant is Viat-Stat. The 510(k) number is K811148.

When did VITA-STAT MODEL 9000-S receive FDA 510(k) clearance?

VITA-STAT MODEL 9000-S received FDA 510(k) clearance on 1981-06-30, under 510(k) number K811148.

Who is the listed applicant for VITA-STAT MODEL 9000-S?

The FDA 510(k) record lists Viat-Stat as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA-STAT MODEL 9000-S?

The FDA product code for VITA-STAT MODEL 9000-S is DSK.

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Related Devices (Code: DSK)

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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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