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FDA 510(k)

ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE

K-Number: K090338 · 2009-05-08

Decision Date2009-05-08
Product CodeMSY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE is the device name listed in this FDA 510(k) record. The listed applicant is Reprocessing Products Corp. It received FDA 510(k) clearance on 2009-05-08 under 510(k) number K090338. The device is classified under product code MSY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE?

ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE is a medical device that received FDA 510(k) clearance on 2009-05-08. The listed applicant is Reprocessing Products Corp. The 510(k) number is K090338.

When did ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE receive FDA 510(k) clearance?

ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE received FDA 510(k) clearance on 2009-05-08, under 510(k) number K090338.

Who is the listed applicant for ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE?

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 ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE?

The FDA product code for ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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