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FDA 510(k)

QLIA IMMUNOCHEMISTRY SYSTEM

K-Number: K883349 · 1988-09-07

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-09-07
Product CodeJZT
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QLIA IMMUNOCHEMISTRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1988-09-07 under 510(k) number K883349. The device is classified under product code JZT. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QLIA IMMUNOCHEMISTRY SYSTEM?

QLIA IMMUNOCHEMISTRY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K883349.

When did QLIA IMMUNOCHEMISTRY SYSTEM receive FDA 510(k) clearance?

QLIA IMMUNOCHEMISTRY SYSTEM received FDA 510(k) clearance on 1988-09-07, under 510(k) number K883349.

Who is the listed applicant for QLIA IMMUNOCHEMISTRY SYSTEM?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QLIA IMMUNOCHEMISTRY SYSTEM?

The FDA product code for QLIA IMMUNOCHEMISTRY SYSTEM is JZT.

Related Clinical Trials

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Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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Related Devices (Code: JZT)

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.

K962499ZYMMUNE AUTOREADER-F FLUORESCENCE MICROPLATE READERBartels, Inc.K882677STAT-20 FLUOROMETERWeaver MedicalK864699FLUORESCENCE CONCENTRATION ANALYZER (FCA)Pandex Laboratories, Inc.K863434THE FIAX 5000 FLUOROMETERWhittaker Bioproducts, Inc.K862674PHOTON ELITE/AUTOMATED RANDOM ACCESS IM/CH SYSTEMHybritech, Inc.K852240SMS, SCREEN MACHINE SYSTEMPandex 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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