FDA 510(k)

8000 SERIES GAS CHROMATOGRAPHS

K-Number: K872122 · 1987-06-17

Decision Date1987-06-17

Product CodeKZQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

8000 SERIES GAS CHROMATOGRAPHS 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 1987-06-17 under 510(k) number K872122. The device is classified under product code KZQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 8000 SERIES GAS CHROMATOGRAPHS?

8000 SERIES GAS CHROMATOGRAPHS is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K872122.

When did 8000 SERIES GAS CHROMATOGRAPHS receive FDA 510(k) clearance?

8000 SERIES GAS CHROMATOGRAPHS received FDA 510(k) clearance on 1987-06-17, under 510(k) number K872122.

Who is the listed applicant for 8000 SERIES GAS CHROMATOGRAPHS?

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 8000 SERIES GAS CHROMATOGRAPHS?

The FDA product code for 8000 SERIES GAS CHROMATOGRAPHS is KZQ.

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Other records listing The Perkin-Elmer Corp. as applicant

K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP K900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.K884864PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO K884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMP K872737PERKIN-ELMER LC235 DIODE ARRAY DETECTOR K872464ION TRAP DETECTOR (ITD)

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Related Devices (Code: KZQ)

K841891VARIAN 3300 & 3400 GAS CHROMATOGRAPHSVarian Assoc., Inc.K832962GAS CHROMATOGRAPH 5890AHewlett-Packard Co.K831387HS-100 HEADSPACE SAMPLING ACCESSORYThe Perkin-Elmer Corp.K830147SIGMA 300 GAS CHROMATROGRAPHThe Perkin-Elmer Corp.K820283SIGMA 2000 GAS CHROMATOGRAPHThe Perkin-Elmer Corp.K820025TRACE ANALYTICAL REDUCTION GAS ANALYZTrace Analytical

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.