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FDA 510(k)

PRE-CALIBRATED PIPETTES

K-Number: K834100 · 1984-02-21

ApplicantVitex
Decision Date1984-02-21
Product CodeJRC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRE-CALIBRATED PIPETTES is the device name listed in this FDA 510(k) record. The listed applicant is Vitex. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834100. The device is classified under product code JRC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-CALIBRATED PIPETTES?

PRE-CALIBRATED PIPETTES is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Vitex. The 510(k) number is K834100.

When did PRE-CALIBRATED PIPETTES receive FDA 510(k) clearance?

PRE-CALIBRATED PIPETTES received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834100.

Who is the listed applicant for PRE-CALIBRATED PIPETTES?

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

What is the FDA product code for PRE-CALIBRATED PIPETTES?

The FDA product code for PRE-CALIBRATED PIPETTES is JRC.

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Related Devices (Code: JRC)

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.

K840186SMI DIGITRONScientific Manufacturing IndustriesK822078DADE DISP. DISPENSING-SPREADING PIPETSAmerican DadeK792696MICROPITETTEMeridian Diagnostics, Inc.K770594LABORATORY EXPENDABLE PRODUCTSAbco Dealers, Inc.K760621LANCER PLASTIC TRANSFER PIPETTESherwood Medical Industries

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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