DEVILBISS MODEL 8500D
K-Number: K874041 · 1987-12-23
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Device Summary
Frequently Asked Questions
What is the DEVILBISS MODEL 8500D?
DEVILBISS MODEL 8500D is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is The Devilbiss Co.. The 510(k) number is K874041.
When did DEVILBISS MODEL 8500D receive FDA 510(k) clearance?
DEVILBISS MODEL 8500D received FDA 510(k) clearance on 1987-12-23, under 510(k) number K874041.
Who is the listed applicant for DEVILBISS MODEL 8500D?
The FDA 510(k) record lists The Devilbiss Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEVILBISS MODEL 8500D?
The FDA product code for DEVILBISS MODEL 8500D is CAF.
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 Devilbiss Co. 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: CAF)
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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