SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST
K-Number: K921099 · 1992-05-29
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Device Summary
Frequently Asked Questions
What is the SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST?
SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST is a medical device that received FDA 510(k) clearance on 1992-05-29. The listed applicant is Syntron Bioresearch, Inc.. The 510(k) number is K921099.
When did SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST receive FDA 510(k) clearance?
SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST received FDA 510(k) clearance on 1992-05-29, under 510(k) number K921099.
Who is the listed applicant for SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST?
The FDA 510(k) record lists Syntron Bioresearch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST?
The FDA product code for SYNTRON QUIKSTRIP/E.Z. STRIP PREGNANCY HOME TEST is LCX.
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 Syntron Bioresearch, 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: LCX)
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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