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FDA 510(k)

CENTRIFICHEM SYSTEM MANAGER

K-Number: K801438 · 1980-07-28

ApplicantUnion Carbide Corp.
Decision Date1980-07-28
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIFICHEM SYSTEM MANAGER is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801438. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIFICHEM SYSTEM MANAGER?

CENTRIFICHEM SYSTEM MANAGER is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Union Carbide Corp.. The 510(k) number is K801438.

When did CENTRIFICHEM SYSTEM MANAGER receive FDA 510(k) clearance?

CENTRIFICHEM SYSTEM MANAGER received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801438.

Who is the listed applicant for CENTRIFICHEM SYSTEM MANAGER?

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

What is the FDA product code for CENTRIFICHEM SYSTEM MANAGER?

The FDA product code for CENTRIFICHEM SYSTEM MANAGER is JQP.

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.

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Other records listing Union Carbide Corp. 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.

K830337MARK III OXYGEN WALKER SYS-LOW PRESSK820836MARK III OXYGEN WALKER SYSTEMK820535LASER GAS MIXTURESK812536LINDE MARK IIK810732LINDE MARK II OXYGEN RESERV. TYPE OR-4K810596CENTRIFI CHEM SYSTEM 400 ANALYZER

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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.

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