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FDA 510(k)

SYSMEX CC-780 EIGHT PARAMETER AUT0

K-Number: K834021 · 1984-03-02

ApplicantToa Medical Electronics USA, Inc.
Decision Date1984-03-02
Product Code
DecisionSubstantially Equivalent

Device Summary

SYSMEX CC-780 EIGHT PARAMETER AUT0 is the device name listed in this FDA 510(k) record. The listed applicant is Toa Medical Electronics USA, Inc.. It received FDA 510(k) clearance on 1984-03-02 under 510(k) number K834021. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSMEX CC-780 EIGHT PARAMETER AUT0?

SYSMEX CC-780 EIGHT PARAMETER AUT0 is a medical device that received FDA 510(k) clearance on 1984-03-02. The listed applicant is Toa Medical Electronics USA, Inc.. The 510(k) number is K834021.

When did SYSMEX CC-780 EIGHT PARAMETER AUT0 receive FDA 510(k) clearance?

SYSMEX CC-780 EIGHT PARAMETER AUT0 received FDA 510(k) clearance on 1984-03-02, under 510(k) number K834021.

Who is the listed applicant for SYSMEX CC-780 EIGHT PARAMETER AUT0?

The FDA 510(k) record lists Toa Medical Electronics USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Toa Medical Electronics USA, Inc. 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.

K936023SYSMEX SE-9000 AUTOMATED HEMATOLOGY ANALYZERK933886TOA MEDICAL ELECTRONICS CA-5000K931149CA-1000 AUTOMATED COAGULATION ANALYZERK920544SYSMEX HEMATOLOGY SYSTEM ACCESSORIESK914744SYSMEX NE-1500, MODIFICATIONK912494SYSMEX(TM) R-3000 AUTOMATED RETICULOCYTE ANALYZER

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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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