VIRAFREE CORP. EJECTABLE NEEDLE HOLDER
K-Number: K896293 · 1990-01-18
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Device Summary
Frequently Asked Questions
What is the VIRAFREE CORP. EJECTABLE NEEDLE HOLDER?
VIRAFREE CORP. EJECTABLE NEEDLE HOLDER is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Virafree Corp.. The 510(k) number is K896293.
When did VIRAFREE CORP. EJECTABLE NEEDLE HOLDER receive FDA 510(k) clearance?
VIRAFREE CORP. EJECTABLE NEEDLE HOLDER received FDA 510(k) clearance on 1990-01-18, under 510(k) number K896293.
Who is the listed applicant for VIRAFREE CORP. EJECTABLE NEEDLE HOLDER?
The FDA 510(k) record lists Virafree Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIRAFREE CORP. EJECTABLE NEEDLE HOLDER?
The FDA product code for VIRAFREE CORP. EJECTABLE NEEDLE HOLDER is FMI.
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.
Related Devices (Code: FMI)
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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