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FDA 510(k)

STAC SYSTEM - ADDITIONAL ANALYTES

K-Number: K772352 · 1978-01-31

Decision Date1978-01-31
Product CodeCGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STAC SYSTEM - ADDITIONAL ANALYTES is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1978-01-31 under 510(k) number K772352. The device is classified under product code CGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAC SYSTEM - ADDITIONAL ANALYTES?

STAC SYSTEM - ADDITIONAL ANALYTES is a medical device that received FDA 510(k) clearance on 1978-01-31. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K772352.

When did STAC SYSTEM - ADDITIONAL ANALYTES receive FDA 510(k) clearance?

STAC SYSTEM - ADDITIONAL ANALYTES received FDA 510(k) clearance on 1978-01-31, under 510(k) number K772352.

Who is the listed applicant for STAC SYSTEM - ADDITIONAL ANALYTES?

The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAC SYSTEM - ADDITIONAL ANALYTES?

The FDA product code for STAC SYSTEM - ADDITIONAL ANALYTES is CGS.

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 Technicon Instruments Corp. 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.

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Related Devices (Code: CGS)

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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