VIRTRAN VIRAL TRANSPORTER (MODIFIED)
K-Number: K860967 · 1986-04-04
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Device Summary
Frequently Asked Questions
What is the VIRTRAN VIRAL TRANSPORTER (MODIFIED)?
VIRTRAN VIRAL TRANSPORTER (MODIFIED) is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Diagnon Corp.. The 510(k) number is K860967.
When did VIRTRAN VIRAL TRANSPORTER (MODIFIED) receive FDA 510(k) clearance?
VIRTRAN VIRAL TRANSPORTER (MODIFIED) received FDA 510(k) clearance on 1986-04-04, under 510(k) number K860967.
Who is the listed applicant for VIRTRAN VIRAL TRANSPORTER (MODIFIED)?
The FDA 510(k) record lists Diagnon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIRTRAN VIRAL TRANSPORTER (MODIFIED)?
The FDA product code for VIRTRAN VIRAL TRANSPORTER (MODIFIED) is JSN.
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 Diagnon Corp. 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: JSN)
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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