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FDA 510(k)

TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD

K-Number: K860830 · 1986-09-08

ApplicantTechnicon Instruments Corp.
Decision Date1986-09-08
Product CodeLIZ
Advisory CommitteeHE
DecisionSubstantially Equivalent for Some Indications

Device Summary

TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1986-09-08 under 510(k) number K860830. The device is classified under product code LIZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD?

TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD is a medical device that received FDA 510(k) clearance on 1986-09-08. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K860830.

When did TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD receive FDA 510(k) clearance?

TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD received FDA 510(k) clearance on 1986-09-08, under 510(k) number K860830.

Who is the listed applicant for TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD?

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

What is the FDA product code for TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD?

The FDA product code for TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD is LIZ.

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Related Devices (Code: LIZ)

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.

K914847CD8 MONOCLONAL ANTIBODIESGen Trak, Inc.K843062TBM-REAGENT FOR T,B CELL & MONOCYTESBd Becton Dickinson Vacutainer Systems PreanalyticK842218ANTI-LEU-4 FITC LYSIN C BUFFERBd Becton Dickinson Vacutainer Systems PreanalyticK833929WHITE BLOOD CELLS HUMAN TAND BControl DiagnosticsK831053QUANTIGEN T & B CELL ASSAYBio-RadK820643ORTHO SPECTRUM III & ORTHO-MUNE OKOrtho Diagnostic Systems, 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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