CONTEMPRO-MIST
K-Number: K000543 · 2000-06-16
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Device Summary
Frequently Asked Questions
What is the CONTEMPRO-MIST?
CONTEMPRO-MIST is a medical device that received FDA 510(k) clearance on 2000-06-16. The listed applicant is Contemporary Products, Inc.. The 510(k) number is K000543.
When did CONTEMPRO-MIST receive FDA 510(k) clearance?
CONTEMPRO-MIST received FDA 510(k) clearance on 2000-06-16, under 510(k) number K000543.
Who is the listed applicant for CONTEMPRO-MIST?
The FDA 510(k) record lists Contemporary Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTEMPRO-MIST?
The FDA product code for CONTEMPRO-MIST 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 Contemporary Products, 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.
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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