AUTOSAMPLER, MODEL AS-40
K-Number: K790117 · 1979-03-19
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Device Summary
Frequently Asked Questions
What is the AUTOSAMPLER, MODEL AS-40?
AUTOSAMPLER, MODEL AS-40 is a medical device that received FDA 510(k) clearance on 1979-03-19. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K790117.
When did AUTOSAMPLER, MODEL AS-40 receive FDA 510(k) clearance?
AUTOSAMPLER, MODEL AS-40 received FDA 510(k) clearance on 1979-03-19, under 510(k) number K790117.
Who is the listed applicant for AUTOSAMPLER, MODEL AS-40?
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 AUTOSAMPLER, MODEL AS-40?
The FDA product code for AUTOSAMPLER, MODEL AS-40 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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