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FDA 510(k)

PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP

K-Number: K935666 · 1994-04-26

ApplicantThe Perkin-Elmer Corp.
Decision Date1994-04-26
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP 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 1994-04-26 under 510(k) number K935666. 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 PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP?

PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K935666.

When did PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP receive FDA 510(k) clearance?

PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP received FDA 510(k) clearance on 1994-04-26, under 510(k) number K935666.

Who is the listed applicant for PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP?

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 PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP?

The FDA product code for PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP is KIE.

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Other records listing The Perkin-Elmer Corp. 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 CorporationK924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.K844947EMIT ANCILLARY REAGENTSSyva Co.

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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