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FDA 510(k)

KENLOR LIQUID TOTAL URINE CONTROL

K-Number: K952840 · 1995-07-19

ApplicantKenlor Industries, Inc.
Decision Date1995-07-19
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KENLOR LIQUID TOTAL URINE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Kenlor Industries, Inc.. It received FDA 510(k) clearance on 1995-07-19 under 510(k) number K952840. 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 KENLOR LIQUID TOTAL URINE CONTROL?

KENLOR LIQUID TOTAL URINE CONTROL is a medical device that received FDA 510(k) clearance on 1995-07-19. The listed applicant is Kenlor Industries, Inc.. The 510(k) number is K952840.

When did KENLOR LIQUID TOTAL URINE CONTROL receive FDA 510(k) clearance?

KENLOR LIQUID TOTAL URINE CONTROL received FDA 510(k) clearance on 1995-07-19, under 510(k) number K952840.

Who is the listed applicant for KENLOR LIQUID TOTAL URINE CONTROL?

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

What is the FDA product code for KENLOR LIQUID TOTAL URINE CONTROL?

The FDA product code for KENLOR LIQUID TOTAL URINE CONTROL is JJW.

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Other records listing Kenlor Industries, 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.

K964014KENLOR H. PYLORI CONTROL SERUMK950326KENLOR HUMAN SPINAL FLUID CONTROLK903338KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROLK896440KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KITK890618COOMASSIE BLUE TOTAL PROTEIN ASSAY KITK890573KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT

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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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