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FDA 510(k)

VITA-STAT MODEL 900A

K-Number: K792192 · 1979-11-13

Decision Date1979-11-13
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITA-STAT MODEL 900A is the device name listed in this FDA 510(k) record. The listed applicant is Vita-Stat Medical Services, Inc.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792192. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA-STAT MODEL 900A?

VITA-STAT MODEL 900A is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Vita-Stat Medical Services, Inc.. The 510(k) number is K792192.

When did VITA-STAT MODEL 900A receive FDA 510(k) clearance?

VITA-STAT MODEL 900A received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792192.

Who is the listed applicant for VITA-STAT MODEL 900A?

The FDA 510(k) record lists Vita-Stat Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA-STAT MODEL 900A?

The FDA product code for VITA-STAT MODEL 900A is DXN.

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.

Other records listing Vita-Stat Medical Services, Inc. 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.

Related Devices (Code: DXN)

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.

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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