VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup
K-Number: K252867 · 2025-10-09
Device Summary
Frequently Asked Questions
What is the VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup?
VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup is a medical device that received FDA 510(k) clearance on 2025-10-09. The listed applicant is Advin Biotech, Inc.. The 510(k) number is K252867.
When did VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup receive FDA 510(k) clearance?
VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup received FDA 510(k) clearance on 2025-10-09, under 510(k) number K252867.
Who is the listed applicant for VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup?
The FDA 510(k) record lists Advin Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup?
The FDA product code for VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup is NFT.
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 Advin Biotech, 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: NFT)
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.