MICRO X RESIDUAL TEST STRIPS
K-Number: K974064 · 1998-12-07
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Device Summary
Frequently Asked Questions
What is the MICRO X RESIDUAL TEST STRIPS?
MICRO X RESIDUAL TEST STRIPS is a medical device that received FDA 510(k) clearance on 1998-12-07. The listed applicant is Reprocessing Products Corp. The 510(k) number is K974064.
When did MICRO X RESIDUAL TEST STRIPS receive FDA 510(k) clearance?
MICRO X RESIDUAL TEST STRIPS received FDA 510(k) clearance on 1998-12-07, under 510(k) number K974064.
Who is the listed applicant for MICRO X RESIDUAL TEST STRIPS?
The FDA 510(k) record lists Reprocessing Products Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO X RESIDUAL TEST STRIPS?
The FDA product code for MICRO X RESIDUAL TEST STRIPS is MSY.
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 Reprocessing Products Corp 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: MSY)
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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