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FDA 510(k)

MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS

K-Number: K781010 · 1978-07-27

ApplicantThe Perkin-Elmer Corp.
Decision Date1978-07-27
Product CodeDPH
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS 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 1978-07-27 under 510(k) number K781010. 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 MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS?

MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K781010.

When did MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS receive FDA 510(k) clearance?

MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781010.

Who is the listed applicant for MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS?

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 MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS?

The FDA product code for MERCURY/HYDRIDE ATOMIC ABSORPTION ACCESS is DPH.

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Other records listing The Perkin-Elmer Corp. as applicant

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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.

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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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