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FDA 510(k)

CENTRIFICHEM PIPETTOR ACCURACY CALIB.

K-Number: K802520 · 1980-11-12

ApplicantUnion Carbide Corp.
Decision Date1980-11-12
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIFICHEM PIPETTOR ACCURACY CALIB. 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 1980-11-12 under 510(k) number K802520. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIFICHEM PIPETTOR ACCURACY CALIB.?

CENTRIFICHEM PIPETTOR ACCURACY CALIB. is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Union Carbide Corp.. The 510(k) number is K802520.

When did CENTRIFICHEM PIPETTOR ACCURACY CALIB. receive FDA 510(k) clearance?

CENTRIFICHEM PIPETTOR ACCURACY CALIB. received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802520.

Who is the listed applicant for CENTRIFICHEM PIPETTOR ACCURACY CALIB.?

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 PIPETTOR ACCURACY CALIB.?

The FDA product code for CENTRIFICHEM PIPETTOR ACCURACY CALIB. is JQW.

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Other records listing Union Carbide Corp. as applicant

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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: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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