ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB
K-Number: K810536 · 1981-03-17
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Device Summary
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.
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
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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