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FDA 510(k)

SERIES 10 LIQUID CHROMOTOGRAPH

K-Number: K821727 · 1982-06-22

ApplicantThe Perkin-Elmer Corp.
Decision Date1982-06-22
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERIES 10 LIQUID CHROMOTOGRAPH 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 1982-06-22 under 510(k) number K821727. 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 SERIES 10 LIQUID CHROMOTOGRAPH?

SERIES 10 LIQUID CHROMOTOGRAPH is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K821727.

When did SERIES 10 LIQUID CHROMOTOGRAPH receive FDA 510(k) clearance?

SERIES 10 LIQUID CHROMOTOGRAPH received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821727.

Who is the listed applicant for SERIES 10 LIQUID CHROMOTOGRAPH?

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 SERIES 10 LIQUID CHROMOTOGRAPH?

The FDA product code for SERIES 10 LIQUID CHROMOTOGRAPH is LDM.

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Other records listing The Perkin-Elmer Corp. as applicant

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K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPK900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.K884864PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTROK884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPK872737PERKIN-ELMER LC235 DIODE ARRAY DETECTORK872464ION TRAP DETECTOR (ITD)

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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.

K960392CDMBio-RadK961557ALLIANCE 2690 SEPARATIONS MODULEWaters CorporationK942451BIO-RAD CLINICAL DATA MANAGEMENT SYSTEMBio-RadK922388WATERS(TM) LC MODULE I FOR CLINICAL USEMillipore Corp.K920136WATERS 717 AUTOSAMPLERMillipore Corp.K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETEMillipore 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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