FDA 510(k)

F 900

K-Number: K022054 · 2002-08-06

Decision Date2002-08-06

Product CodeHKY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

F 900 is the device name listed in this FDA 510(k) record. The listed applicant is C.S.O. S.R.L.. It received FDA 510(k) clearance on 2002-08-06 under 510(k) number K022054. The device is classified under product code HKY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F 900?

F 900 is a medical device that received FDA 510(k) clearance on 2002-08-06. The listed applicant is C.S.O. S.R.L.. The 510(k) number is K022054.

When did F 900 receive FDA 510(k) clearance?

F 900 received FDA 510(k) clearance on 2002-08-06, under 510(k) number K022054.

Who is the listed applicant for F 900?

The FDA 510(k) record lists C.S.O. S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F 900?

The FDA product code for F 900 is HKY.

Other records listing C.S.O. S.R.L. 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.

K221601MS-39

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.