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FDA 510(k)

GOLD FILM MERCURY ANALYZER #511

K-Number: K832933 · 1983-11-25

ApplicantJerome Instrument Corp.
Decision Date1983-11-25
Product CodeDPH
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

GOLD FILM MERCURY ANALYZER #511 is the device name listed in this FDA 510(k) record. The listed applicant is Jerome Instrument Corp.. It received FDA 510(k) clearance on 1983-11-25 under 510(k) number K832933. The device is classified under product code DPH. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLD FILM MERCURY ANALYZER #511?

GOLD FILM MERCURY ANALYZER #511 is a medical device that received FDA 510(k) clearance on 1983-11-25. The listed applicant is Jerome Instrument Corp.. The 510(k) number is K832933.

When did GOLD FILM MERCURY ANALYZER #511 receive FDA 510(k) clearance?

GOLD FILM MERCURY ANALYZER #511 received FDA 510(k) clearance on 1983-11-25, under 510(k) number K832933.

Who is the listed applicant for GOLD FILM MERCURY ANALYZER #511?

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

What is the FDA product code for GOLD FILM MERCURY ANALYZER #511?

The FDA product code for GOLD FILM MERCURY ANALYZER #511 is DPH.

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Related Devices (Code: DPH)

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.

K781010MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESSThe Perkin-Elmer Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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