FDA 510(k)

CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT

K-Number: K955154 · 1995-12-11

Decision Date1995-12-11

Product CodeJIX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Alko Diagnostic Corp.. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K955154. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT?

CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Alko Diagnostic Corp.. The 510(k) number is K955154.

When did CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT receive FDA 510(k) clearance?

CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT received FDA 510(k) clearance on 1995-12-11, under 510(k) number K955154.

Who is the listed applicant for CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT?

The FDA 510(k) record lists Alko Diagnostic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT?

The FDA product code for CAL 1 & CAL 2 SOLUTION, FLUSH SOLUTION KIT is JIX.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Alko Diagnostic Corp. as applicant

K001484CALIBRATION SOLUTION 1, MODEL A943-837; CALIBRATION SOLUTION 2, MODEL A943-839; RINSE SOLUTION KIT, MODEL A943-838 K982501ELECTROLYTE BUFFER A443-325, ELECTROLYTE REFERENCE REAGENT A443-315, CO2 ACID REAGENT A443-330, CO2 ALKALINE BUFFER A44 K972004ISE REAGENTS FOR OLYMPUS AU 800/AU5200 CHEMISTRY SYSTEMS K970921STANDARD A MULTIPLY (A540-0), STANDARD B MULTIPLY (A550-0), STANDARD C MULTIPLY (A560-0)K962864THB CAL STANDARD FOR IL CO-OXIMETERS/OXIMETERS K963734ISE REAGENTS FOR HITACHI 700 SERIES AND 911 CLINICAL CHEMISTRY SYSTEMS

View all 31 devices →

Related Devices (Code: JIX)

K161140VITROS Chemistry Products Calibrator Kit 3Ortho-Clinical Diagnostics, Inc.K133330C.F.A.S. PROTEINS, C.F.A.S. PAC, PRECICONTROL CLINCHEM MULTI 1 & 2, PRECINORM PROTEIN & PRECIPATH PROTEINRoche Diagnostics K130765ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH CLINICAL SYSTEMS ELITROL I, ELITECH CLINICAL SYSTEMS ELITROL IIElitechgroup K123321DIMENSION CHEMISTRY III CALIBRATORYSiemens Healthcare Diagnostics K123372ABBOTT LIPID MULTI CONSTITUENT CALIBRATORAbbott Laboratories K122398RAPIDPOINT 500 SYSTEM MEASUREMENT CARTRIDGE WITH CALIBRATORSSiemens Healthcare Diagnostics, Inc.

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.