ATOMIZER, FURNACE, GRAPHITE
K-Number: K780129 · 1978-04-05
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Device Summary
Frequently Asked Questions
What is the ATOMIZER, FURNACE, GRAPHITE?
ATOMIZER, FURNACE, GRAPHITE is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K780129.
When did ATOMIZER, FURNACE, GRAPHITE receive FDA 510(k) clearance?
ATOMIZER, FURNACE, GRAPHITE received FDA 510(k) clearance on 1978-04-05, under 510(k) number K780129.
Who is the listed applicant for ATOMIZER, FURNACE, GRAPHITE?
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 ATOMIZER, FURNACE, GRAPHITE?
The FDA product code for ATOMIZER, FURNACE, GRAPHITE 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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