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FDA 510(k)

MICROJET CRONO H

K-Number: K013855 · 2002-05-09

ApplicantCane S.R.I.
Decision Date2002-05-09
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROJET CRONO H is the device name listed in this FDA 510(k) record. The listed applicant is Cane S.R.I.. It received FDA 510(k) clearance on 2002-05-09 under 510(k) number K013855. 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 H?

MICROJET CRONO H is a medical device that received FDA 510(k) clearance on 2002-05-09. The listed applicant is Cane S.R.I.. The 510(k) number is K013855.

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

MICROJET CRONO H received FDA 510(k) clearance on 2002-05-09, under 510(k) number K013855.

Who is the listed applicant for MICROJET CRONO H?

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

What is the FDA product code for MICROJET CRONO H?

The FDA product code for MICROJET CRONO H is FRN.

Related Clinical Trials

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Other records listing Cane S.R.I. 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.

K013776MICROJET MODEL # CD4 AND CD4/20

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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