INSTANT-VIEW TROPONIN I TEST
K-Number: K042227 · 2004-11-19
Advertisement
Device Summary
Frequently Asked Questions
What is the INSTANT-VIEW TROPONIN I TEST?
INSTANT-VIEW TROPONIN I TEST is a medical device that received FDA 510(k) clearance on 2004-11-19. The listed applicant is Alfa Scientific Designs, Inc.. The 510(k) number is K042227.
When did INSTANT-VIEW TROPONIN I TEST receive FDA 510(k) clearance?
INSTANT-VIEW TROPONIN I TEST received FDA 510(k) clearance on 2004-11-19, under 510(k) number K042227.
Who is the listed applicant for INSTANT-VIEW TROPONIN I TEST?
The FDA 510(k) record lists Alfa Scientific Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSTANT-VIEW TROPONIN I TEST?
The FDA product code for INSTANT-VIEW TROPONIN I TEST is MMI.
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 Alfa Scientific Designs, 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: MMI)
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.
Advertisement