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FDA 510(k)

STERICHEK BICARB PH REAGENT STRIPS

K-Number: K031267 · 2003-12-23

Decision Date2003-12-23
Product CodeMNV
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STERICHEK BICARB PH REAGENT STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Environmental Test Systems, Inc.. It received FDA 510(k) clearance on 2003-12-23 under 510(k) number K031267. The device is classified under product code MNV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERICHEK BICARB PH REAGENT STRIPS?

STERICHEK BICARB PH REAGENT STRIPS is a medical device that received FDA 510(k) clearance on 2003-12-23. The listed applicant is Environmental Test Systems, Inc.. The 510(k) number is K031267.

When did STERICHEK BICARB PH REAGENT STRIPS receive FDA 510(k) clearance?

STERICHEK BICARB PH REAGENT STRIPS received FDA 510(k) clearance on 2003-12-23, under 510(k) number K031267.

Who is the listed applicant for STERICHEK BICARB PH REAGENT STRIPS?

The FDA 510(k) record lists Environmental Test Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERICHEK BICARB PH REAGENT STRIPS?

The FDA product code for STERICHEK BICARB PH REAGENT STRIPS is MNV.

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 Environmental Test Systems, 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.

View all 8 devices →

Related Devices (Code: MNV)

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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