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FDA 510(k)

CRONO SUPER PID

K-Number: K052217 · 2005-09-13

ApplicantCane S.R.L.
Decision Date2005-09-13
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRONO SUPER PID 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 2005-09-13 under 510(k) number K052217. 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 SUPER PID?

CRONO SUPER PID is a medical device that received FDA 510(k) clearance on 2005-09-13. The listed applicant is Cane S.R.L.. The 510(k) number is K052217.

When did CRONO SUPER PID receive FDA 510(k) clearance?

CRONO SUPER PID received FDA 510(k) clearance on 2005-09-13, under 510(k) number K052217.

Who is the listed applicant for CRONO SUPER PID?

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 SUPER PID?

The FDA product code for CRONO SUPER PID 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.

K091042CRONO S-PID 50K052218CRONO FIVE AND CRONO PCA 50K052219CRONO GO.K042085CRONO FK041414CRONO AND CRONO, MODEL 30K013840MICROJET CRONO PAR AND CRONO APO-GO

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Related Devices (Code: FRN)

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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