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FDA 510(k)

CANTROL ELECTROPHORESIS CONTROL

K-Number: K854931 · 1986-01-17

ApplicantCanyon Diagnostics, Inc.
Decision Date1986-01-17
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CANTROL ELECTROPHORESIS CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Canyon Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-01-17 under 510(k) number K854931. 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 CANTROL ELECTROPHORESIS CONTROL?

CANTROL ELECTROPHORESIS CONTROL is a medical device that received FDA 510(k) clearance on 1986-01-17. The listed applicant is Canyon Diagnostics, Inc.. The 510(k) number is K854931.

When did CANTROL ELECTROPHORESIS CONTROL receive FDA 510(k) clearance?

CANTROL ELECTROPHORESIS CONTROL received FDA 510(k) clearance on 1986-01-17, under 510(k) number K854931.

Who is the listed applicant for CANTROL ELECTROPHORESIS CONTROL?

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

What is the FDA product code for CANTROL ELECTROPHORESIS CONTROL?

The FDA product code for CANTROL ELECTROPHORESIS CONTROL is JJY.

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Other records listing Canyon Diagnostics, 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.

K970248CANTROL SERUM IRON AND TOTAL IRON BINDING CAPACITY TEST SYSTEMK964640CANTROL IRON/TIBC CONTROLS, LEVEL 1 AND LEVEL 2 PRODUCT NUMBERS: LEVEL 1: IIBC-91 AND LEVEL 2: IIBC-92K882488CANTROL HDL CHOLESTEROL PRECIPI. REAG. AND TUBESK871537CANTROL HDL CHOLESTROL CONTROLS LEVELS I AND IIK855006CANTROL CK/MB CONTROLK854190CANTROL SPINAL FLUID CONTROL

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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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