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FDA 510(k)

CORSINI 9090

K-Number: K950402 · 1995-03-31

ApplicantC.A.T. DI Corsini G. & C. Spa
Decision Date1995-03-31
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORSINI 9090 is the device name listed in this FDA 510(k) record. The listed applicant is C.A.T. DI Corsini G. & C. Spa. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K950402. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORSINI 9090?

CORSINI 9090 is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is C.A.T. DI Corsini G. & C. Spa. The 510(k) number is K950402.

When did CORSINI 9090 receive FDA 510(k) clearance?

CORSINI 9090 received FDA 510(k) clearance on 1995-03-31, under 510(k) number K950402.

Who is the listed applicant for CORSINI 9090?

The FDA 510(k) record lists C.A.T. DI Corsini G. & C. Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORSINI 9090?

The FDA product code for CORSINI 9090 is IXR.

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Related Devices (Code: IXR)

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.

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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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