ANALYSIS SYSTEM, PREP SAMPLE
K-Number: K781941 · 1979-01-03
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Device Summary
Frequently Asked Questions
What is the ANALYSIS SYSTEM, PREP SAMPLE?
ANALYSIS SYSTEM, PREP SAMPLE is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K781941.
When did ANALYSIS SYSTEM, PREP SAMPLE receive FDA 510(k) clearance?
ANALYSIS SYSTEM, PREP SAMPLE received FDA 510(k) clearance on 1979-01-03, under 510(k) number K781941.
Who is the listed applicant for ANALYSIS SYSTEM, PREP SAMPLE?
The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANALYSIS SYSTEM, PREP SAMPLE?
The FDA product code for ANALYSIS SYSTEM, PREP SAMPLE is DOZ.
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 E.I. Dupont DE Nemours & Co., Inc. 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.
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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