Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AUTOSAMPLER, MODEL AS-40

K-Number: K790117 · 1979-03-19

Decision Date1979-03-19
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOSAMPLER, MODEL AS-40 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 1979-03-19 under 510(k) number K790117. 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 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑