AM-40 SYSTEM
K-Number: K821715 · 1982-06-25
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Device Summary
Frequently Asked Questions
What is the AM-40 SYSTEM?
AM-40 SYSTEM is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is American Midwest. The 510(k) number is K821715.
When did AM-40 SYSTEM receive FDA 510(k) clearance?
AM-40 SYSTEM received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821715.
Who is the listed applicant for AM-40 SYSTEM?
The FDA 510(k) record lists American Midwest as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AM-40 SYSTEM?
The FDA product code for AM-40 SYSTEM is EFB.
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 American Midwest 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: EFB)
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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