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FDA 510(k)

QUIX RAPID CHOLERA STRIP TEST

K-Number: K954995 · 1996-08-15

ApplicantGuardian Scientific, Corp.
Decision Date1996-08-15
Product CodeGSQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUIX RAPID CHOLERA STRIP TEST is the device name listed in this FDA 510(k) record. The listed applicant is Guardian Scientific, Corp.. It received FDA 510(k) clearance on 1996-08-15 under 510(k) number K954995. The device is classified under product code GSQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIX RAPID CHOLERA STRIP TEST?

QUIX RAPID CHOLERA STRIP TEST is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Guardian Scientific, Corp.. The 510(k) number is K954995.

When did QUIX RAPID CHOLERA STRIP TEST receive FDA 510(k) clearance?

QUIX RAPID CHOLERA STRIP TEST received FDA 510(k) clearance on 1996-08-15, under 510(k) number K954995.

Who is the listed applicant for QUIX RAPID CHOLERA STRIP TEST?

The FDA 510(k) record lists Guardian Scientific, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUIX RAPID CHOLERA STRIP TEST?

The FDA product code for QUIX RAPID CHOLERA STRIP TEST is GSQ.

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Other records listing Guardian Scientific, 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.

K972156QUIX RAPID E. COLI O157 STRIP TESTK954994TRUSTK954993QUIX RAPID PREGNANCY STRIP TEST

Related Devices (Code: GSQ)

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.

K932622CHOLERA SMART(TM)New Horizons Diagnostics Co.K922432CHOLERASCREENNew Horizons Diagnostics Co.

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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