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FDA 510(k)

SERIES 4 LIQUID CHROMATOGRAPH

K-Number: K821219 · 1982-05-28

ApplicantThe Perkin-Elmer Corp.
Decision Date1982-05-28
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERIES 4 LIQUID CHROMATOGRAPH 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 1982-05-28 under 510(k) number K821219. 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 4 LIQUID CHROMATOGRAPH?

SERIES 4 LIQUID CHROMATOGRAPH is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K821219.

When did SERIES 4 LIQUID CHROMATOGRAPH receive FDA 510(k) clearance?

SERIES 4 LIQUID CHROMATOGRAPH received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821219.

Who is the listed applicant for SERIES 4 LIQUID CHROMATOGRAPH?

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 4 LIQUID CHROMATOGRAPH?

The FDA product code for SERIES 4 LIQUID CHROMATOGRAPH is LDM.

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Other records listing The Perkin-Elmer Corp. as applicant

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.

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.

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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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