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FDA 510(k)

MICROJET CRONO PCA

K-Number: K013822 · 2002-05-08

ApplicantCane S.R.L.
Decision Date2002-05-08
Product CodeMEA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROJET CRONO PCA 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 2002-05-08 under 510(k) number K013822. The device is classified under product code MEA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROJET CRONO PCA?

MICROJET CRONO PCA is a medical device that received FDA 510(k) clearance on 2002-05-08. The listed applicant is Cane S.R.L.. The 510(k) number is K013822.

When did MICROJET CRONO PCA receive FDA 510(k) clearance?

MICROJET CRONO PCA received FDA 510(k) clearance on 2002-05-08, under 510(k) number K013822.

Who is the listed applicant for MICROJET CRONO PCA?

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 MICROJET CRONO PCA?

The FDA product code for MICROJET CRONO PCA is MEA.

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Other records listing Cane S.R.L. as applicant

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Related Devices (Code: MEA)

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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