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FDA 510(k)

MODEL 5000, LIQUID CHROMATOGRAPHY

K-Number: K781379 · 1978-09-14

ApplicantVarian Assoc., Inc.
Decision Date1978-09-14
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 5000, LIQUID CHROMATOGRAPHY is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781379. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 5000, LIQUID CHROMATOGRAPHY?

MODEL 5000, LIQUID CHROMATOGRAPHY is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K781379.

When did MODEL 5000, LIQUID CHROMATOGRAPHY receive FDA 510(k) clearance?

MODEL 5000, LIQUID CHROMATOGRAPHY received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781379.

Who is the listed applicant for MODEL 5000, LIQUID CHROMATOGRAPHY?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 5000, LIQUID CHROMATOGRAPHY?

The FDA product code for MODEL 5000, LIQUID CHROMATOGRAPHY is KIE.

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Other records listing Varian Assoc., Inc. as applicant

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Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.

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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