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FDA 510(k)

TECHNICON H6000 SYSTEM CONTROL

K-Number: K831704 · 1983-07-06

ApplicantTechnicon Instruments Corp.
Decision Date1983-07-06
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TECHNICON H6000 SYSTEM CONTROL 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 1983-07-06 under 510(k) number K831704. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON H6000 SYSTEM CONTROL?

TECHNICON H6000 SYSTEM CONTROL is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K831704.

When did TECHNICON H6000 SYSTEM CONTROL receive FDA 510(k) clearance?

TECHNICON H6000 SYSTEM CONTROL received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831704.

Who is the listed applicant for TECHNICON H6000 SYSTEM CONTROL?

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 H6000 SYSTEM CONTROL?

The FDA product code for TECHNICON H6000 SYSTEM CONTROL is JPK.

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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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