ACCUSCREEN T4
K-Number: K781222 · 1978-11-08
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Device Summary
Frequently Asked Questions
What is the ACCUSCREEN T4?
ACCUSCREEN T4 is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Neometrics, Inc.. The 510(k) number is K781222.
When did ACCUSCREEN T4 receive FDA 510(k) clearance?
ACCUSCREEN T4 received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781222.
Who is the listed applicant for ACCUSCREEN T4?
The FDA 510(k) record lists Neometrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUSCREEN T4?
The FDA product code for ACCUSCREEN T4 is CDX.
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 Neometrics, 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.
Related Devices (Code: CDX)
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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