ATOMISOR
K-Number: K970844 · 1997-11-13
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Device Summary
Frequently Asked Questions
What is the ATOMISOR?
ATOMISOR is a medical device that received FDA 510(k) clearance on 1997-11-13. The listed applicant is Medical Consulting Service, Inc.. The 510(k) number is K970844.
When did ATOMISOR receive FDA 510(k) clearance?
ATOMISOR received FDA 510(k) clearance on 1997-11-13, under 510(k) number K970844.
Who is the listed applicant for ATOMISOR?
The FDA 510(k) record lists Medical Consulting Service, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATOMISOR?
The FDA product code for ATOMISOR 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.
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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