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FDA 510(k)

KOVA LIQUA-TROL

K-Number: K942853 · 1994-10-04

ApplicantHycor Biomedical, Inc.
Decision Date1994-10-04
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KOVA LIQUA-TROL is the device name listed in this FDA 510(k) record. The listed applicant is Hycor Biomedical, Inc.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K942853. 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 LIQUA-TROL?

KOVA LIQUA-TROL is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K942853.

When did KOVA LIQUA-TROL receive FDA 510(k) clearance?

KOVA LIQUA-TROL received FDA 510(k) clearance on 1994-10-04, under 510(k) number K942853.

Who is the listed applicant for KOVA LIQUA-TROL?

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

What is the FDA product code for KOVA LIQUA-TROL?

The FDA product code for KOVA LIQUA-TROL is JJW.

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Other records listing Hycor Biomedical, Inc. as applicant

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Related Devices (Code: JJW)

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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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