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FDA 510(k)

LIQUID CHROMATOGRAPH 1090 SERIES

K-Number: K832375 · 1983-10-14

ApplicantHewlett-Packard Co.
Decision Date1983-10-14
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHROMATOGRAPH 1090 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832375. The device is classified under product code LDM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHROMATOGRAPH 1090 SERIES?

LIQUID CHROMATOGRAPH 1090 SERIES is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K832375.

When did LIQUID CHROMATOGRAPH 1090 SERIES receive FDA 510(k) clearance?

LIQUID CHROMATOGRAPH 1090 SERIES received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832375.

Who is the listed applicant for LIQUID CHROMATOGRAPH 1090 SERIES?

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

What is the FDA product code for LIQUID CHROMATOGRAPH 1090 SERIES?

The FDA product code for LIQUID CHROMATOGRAPH 1090 SERIES is LDM.

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Related Devices (Code: LDM)

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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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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