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FDA 510(k)

CRONO S-PID 50

K-Number: K091042 · 2009-05-12

ApplicantCane S.R.L.
Decision Date2009-05-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRONO S-PID 50 is the device name listed in this FDA 510(k) record. The listed applicant is Cane S.R.L.. It received FDA 510(k) clearance on 2009-05-12 under 510(k) number K091042. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRONO S-PID 50?

CRONO S-PID 50 is a medical device that received FDA 510(k) clearance on 2009-05-12. The listed applicant is Cane S.R.L.. The 510(k) number is K091042.

When did CRONO S-PID 50 receive FDA 510(k) clearance?

CRONO S-PID 50 received FDA 510(k) clearance on 2009-05-12, under 510(k) number K091042.

Who is the listed applicant for CRONO S-PID 50?

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

What is the FDA product code for CRONO S-PID 50?

The FDA product code for CRONO S-PID 50 is FRN.

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Other records listing Cane 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.

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Related Devices (Code: FRN)

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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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