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FDA 510(k)

HGA-2200 HEATED GRAPHITE ATOMIZER

K-Number: K761317 · 1977-02-07

ApplicantThe Perkin-Elmer Corp.
Decision Date1977-02-07
Product Code
DecisionSubstantially Equivalent

Device Summary

HGA-2200 HEATED GRAPHITE ATOMIZER 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 1977-02-07 under 510(k) number K761317. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HGA-2200 HEATED GRAPHITE ATOMIZER?

HGA-2200 HEATED GRAPHITE ATOMIZER is a medical device that received FDA 510(k) clearance on 1977-02-07. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K761317.

When did HGA-2200 HEATED GRAPHITE ATOMIZER receive FDA 510(k) clearance?

HGA-2200 HEATED GRAPHITE ATOMIZER received FDA 510(k) clearance on 1977-02-07, under 510(k) number K761317.

Who is the listed applicant for HGA-2200 HEATED GRAPHITE ATOMIZER?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

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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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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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