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FDA 510(k)

KOVA STRIP 6

K-Number: K811219 · 1981-05-21

ApplicantIcl Scientific
Decision Date1981-05-21
Product CodeJIR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KOVA STRIP 6 is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K811219. The device is classified under product code JIR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOVA STRIP 6?

KOVA STRIP 6 is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Icl Scientific. The 510(k) number is K811219.

When did KOVA STRIP 6 receive FDA 510(k) clearance?

KOVA STRIP 6 received FDA 510(k) clearance on 1981-05-21, under 510(k) number K811219.

Who is the listed applicant for KOVA STRIP 6?

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

What is the FDA product code for KOVA STRIP 6?

The FDA product code for KOVA STRIP 6 is JIR.

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Other records listing Icl Scientific 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.

K883942HYCOR SENTRY DRUGS OF ABUSE URINE CONTROLK843565KOVA TROL I,II, III HUMAN URINE-DRIEDK833761THERAPEUTIC DRUG CONTROLK832823ENZYMUNE-TEST TSHK831383EVENT-TEST SLIDEK823199ENZYME-TEST DIGOXIN

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Related Devices (Code: JIR)

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.

K222921Minuteful-kidney testHealthy.Io, Ltd.K210069Minuteful - kidney testHealthy.Io, Ltd.K061419TECO MICROALBUMIN 2-1 COMBO STRIPSTeco DiagnosticsK022538IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25Diagnostic Chemicals, Ltd. (Usa)K001810URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTINGFlexsite Diagnostics, Inc.K994035IMMUNODIP URINARY ALBUMIN SCREEN, MODEL 790-01, 790-15Diagnostic Chemicals , Ltd.

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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