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FDA 510(k)

LIQUID CHROMATOGRAPH 400

K-Number: K843568 · 1984-11-20

Decision Date1984-11-20
Product CodeKZR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHROMATOGRAPH 400 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 1984-11-20 under 510(k) number K843568. The device is classified under product code KZR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHROMATOGRAPH 400?

LIQUID CHROMATOGRAPH 400 is a medical device that received FDA 510(k) clearance on 1984-11-20. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K843568.

When did LIQUID CHROMATOGRAPH 400 receive FDA 510(k) clearance?

LIQUID CHROMATOGRAPH 400 received FDA 510(k) clearance on 1984-11-20, under 510(k) number K843568.

Who is the listed applicant for LIQUID CHROMATOGRAPH 400?

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 LIQUID CHROMATOGRAPH 400?

The FDA product code for LIQUID CHROMATOGRAPH 400 is KZR.

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: KZR)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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