MICROJET MODEL # CD4 AND CD4/20
K-Number: K013776 · 2002-04-26
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Device Summary
Frequently Asked Questions
What is the MICROJET MODEL # CD4 AND CD4/20?
MICROJET MODEL # CD4 AND CD4/20 is a medical device that received FDA 510(k) clearance on 2002-04-26. The listed applicant is Cane S.R.I.. The 510(k) number is K013776.
When did MICROJET MODEL # CD4 AND CD4/20 receive FDA 510(k) clearance?
MICROJET MODEL # CD4 AND CD4/20 received FDA 510(k) clearance on 2002-04-26, under 510(k) number K013776.
Who is the listed applicant for MICROJET MODEL # CD4 AND CD4/20?
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 MODEL # CD4 AND CD4/20?
The FDA product code for MICROJET MODEL # CD4 AND CD4/20 is FRN.
Related Clinical Trials
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.
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.
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.
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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