VENTRESCREEN HCG URINE
K-Number: K853748 · 1985-10-01
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Device Summary
Frequently Asked Questions
What is the VENTRESCREEN HCG URINE?
VENTRESCREEN HCG URINE is a medical device that received FDA 510(k) clearance on 1985-10-01. The listed applicant is Vxr, Inc.. The 510(k) number is K853748.
When did VENTRESCREEN HCG URINE receive FDA 510(k) clearance?
VENTRESCREEN HCG URINE received FDA 510(k) clearance on 1985-10-01, under 510(k) number K853748.
Who is the listed applicant for VENTRESCREEN HCG URINE?
The FDA 510(k) record lists Vxr, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENTRESCREEN HCG URINE?
The FDA product code for VENTRESCREEN HCG URINE is JHI.
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 Vxr, 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: JHI)
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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