Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CVT VIRAL TRANSPORTS

K-Number: K830250 · 1983-02-28

ApplicantImmulok, Inc.
Decision Date1983-02-28
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CVT VIRAL TRANSPORTS is the device name listed in this FDA 510(k) record. The listed applicant is Immulok, Inc.. It received FDA 510(k) clearance on 1983-02-28 under 510(k) number K830250. The device is classified under product code JTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CVT VIRAL TRANSPORTS?

CVT VIRAL TRANSPORTS is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is Immulok, Inc.. The 510(k) number is K830250.

When did CVT VIRAL TRANSPORTS receive FDA 510(k) clearance?

CVT VIRAL TRANSPORTS received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830250.

Who is the listed applicant for CVT VIRAL TRANSPORTS?

The FDA 510(k) record lists Immulok, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CVT VIRAL TRANSPORTS?

The FDA product code for CVT VIRAL TRANSPORTS is JTW.

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 Immulok, Inc. 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.

View all 15 devices →

Related Devices (Code: JTW)

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.

↑