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FDA 510(k)

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID

K-Number: K890576 · 1989-03-09

ApplicantKenlor Industries, Inc.
Decision Date1989-03-09
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID 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 1989-03-09 under 510(k) number K890576. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENLOR HUMAN SPINAL FLUID CONTROL LIQUID?

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID is a medical device that received FDA 510(k) clearance on 1989-03-09. The listed applicant is Kenlor Industries, Inc.. The 510(k) number is K890576.

When did KENLOR HUMAN SPINAL FLUID CONTROL LIQUID receive FDA 510(k) clearance?

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID received FDA 510(k) clearance on 1989-03-09, under 510(k) number K890576.

Who is the listed applicant for KENLOR HUMAN SPINAL FLUID CONTROL LIQUID?

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 HUMAN SPINAL FLUID CONTROL LIQUID?

The FDA product code for KENLOR HUMAN SPINAL FLUID CONTROL LIQUID is JJY.

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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 SERUMK952840KENLOR LIQUID TOTAL URINE CONTROLK950326KENLOR HUMAN SPINAL FLUID CONTROLK903338KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROLK896440KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KITK890618COOMASSIE BLUE TOTAL PROTEIN ASSAY KIT

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Related Devices (Code: JJY)

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.

K162530Multichem IA PlusTechno-Path ManufacturingK163629Audit MicroControls Linearity FD Tumor Markers IIAalto Scientific, Ltd.K163015Liquichek Tumor Marker Control-Level 1; Liquichek Tumor Marker Control-Level 2; Liquichek Tumor Marker Control-Level 3; Liquichek Tumor Marker Control- Trilevel MiniPakBio-Rad LaboratoriesK153712VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification KitRadiometer America, Inc.K132227LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAYBio-Rad LaboratoriesK132156RANDOX CSF CONTROLS LEVELS 2 AND 3Randox Laboratories, 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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