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FDA 510(k)

MICROJET CRONO PAR AND CRONO APO-GO

K-Number: K013840 · 2002-05-14

ApplicantCane S.R.L.
Decision Date2002-05-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROJET CRONO PAR AND CRONO APO-GO 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 2002-05-14 under 510(k) number K013840. 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 MICROJET CRONO PAR AND CRONO APO-GO?

MICROJET CRONO PAR AND CRONO APO-GO is a medical device that received FDA 510(k) clearance on 2002-05-14. The listed applicant is Cane S.R.L.. The 510(k) number is K013840.

When did MICROJET CRONO PAR AND CRONO APO-GO receive FDA 510(k) clearance?

MICROJET CRONO PAR AND CRONO APO-GO received FDA 510(k) clearance on 2002-05-14, under 510(k) number K013840.

Who is the listed applicant for MICROJET CRONO PAR AND CRONO APO-GO?

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 PAR AND CRONO APO-GO?

The FDA product code for MICROJET CRONO PAR AND CRONO APO-GO is 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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