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FDA 510(k)

KOVA TROL I,II, III HUMAN URINE-DRIED

K-Number: K843565 · 1984-10-05

ApplicantIcl Scientific
Decision Date1984-10-05
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KOVA TROL I,II, III HUMAN URINE-DRIED is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1984-10-05 under 510(k) number K843565. The device is classified under product code JJW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOVA TROL I,II, III HUMAN URINE-DRIED?

KOVA TROL I,II, III HUMAN URINE-DRIED is a medical device that received FDA 510(k) clearance on 1984-10-05. The listed applicant is Icl Scientific. The 510(k) number is K843565.

When did KOVA TROL I,II, III HUMAN URINE-DRIED receive FDA 510(k) clearance?

KOVA TROL I,II, III HUMAN URINE-DRIED received FDA 510(k) clearance on 1984-10-05, under 510(k) number K843565.

Who is the listed applicant for KOVA TROL I,II, III HUMAN URINE-DRIED?

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 TROL I,II, III HUMAN URINE-DRIED?

The FDA product code for KOVA TROL I,II, III HUMAN URINE-DRIED is JJW.

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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 CONTROLK833761THERAPEUTIC DRUG CONTROLK832823ENZYMUNE-TEST TSHK831383EVENT-TEST SLIDEK823199ENZYME-TEST DIGOXINK822346HISTIMUNE ENZYME-ANA TEST

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Related Devices (Code: JJW)

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.

K170091UA-Cellular CompleteStreckK110846RANDOX URINALYSIS CONTROLS, LEVELS 1 AND 2Randox Laboratories LimitedK103387MISSION LIQUID URINE CONTROL, MISSION LIQUID DIPTUBE URINE CONTROL, MISSION DRY STRIP URINE CONTROLACON Laboratories, Inc.K081908CLINIQA LIQUID QC URINALYSIS CONTROLS, LEVELS 1 AND 2Cliniqa CorporationK072640IRISPEC,CA/CB/CCIris DiagnosticsK070848LIQUICHEK URINALYSIS CONTROL (BI-LEVEL), CONTROL LEVEL1, LEVEL 2,MINIPAK, 435,436,437,435XBio-Rad, Diagnostics Grp.

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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