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FDA 510(k)

DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.

K-Number: K800516 · 1980-03-19

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1980-03-19
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM. is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1980-03-19 under 510(k) number K800516. 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 DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.?

DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM. is a medical device that received FDA 510(k) clearance on 1980-03-19. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K800516.

When did DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM. receive FDA 510(k) clearance?

DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM. received FDA 510(k) clearance on 1980-03-19, under 510(k) number K800516.

Who is the listed applicant for DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.?

The FDA product code for DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM. is KIE.

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Other records listing E.I. Dupont DE Nemours & Co., 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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