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FDA 510(k)

SIGMA 300 GAS CHROMATROGRAPH

K-Number: K830147 · 1983-02-07

Decision Date1983-02-07
Product CodeKZQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SIGMA 300 GAS CHROMATROGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K830147. The device is classified under product code KZQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGMA 300 GAS CHROMATROGRAPH?

SIGMA 300 GAS CHROMATROGRAPH is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K830147.

When did SIGMA 300 GAS CHROMATROGRAPH receive FDA 510(k) clearance?

SIGMA 300 GAS CHROMATROGRAPH received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830147.

Who is the listed applicant for SIGMA 300 GAS CHROMATROGRAPH?

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

What is the FDA product code for SIGMA 300 GAS CHROMATROGRAPH?

The FDA product code for SIGMA 300 GAS CHROMATROGRAPH is KZQ.

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 The Perkin-Elmer 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.

View all 62 devices →

Related Devices (Code: KZQ)

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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