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FDA 510(k)

ATOMISOR

K-Number: K970844 · 1997-11-13

Decision Date1997-11-13
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ATOMISOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Consulting Service, Inc.. It received FDA 510(k) clearance on 1997-11-13 under 510(k) number K970844. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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