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FDA 510(k)

ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB

K-Number: K810536 · 1981-03-17

Decision Date1981-03-17
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB 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 1981-03-17 under 510(k) number K810536. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB?

ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K810536.

When did ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB receive FDA 510(k) clearance?

ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810536.

Who is the listed applicant for ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB?

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 ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB?

The FDA product code for ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB is JXR.

Related Clinical Trials

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.

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.

View all 62 devices →

Related Devices (Code: JXR)

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.

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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