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FDA 510(k)

TECHNICON RA-1000 SYS-ISE MODULE &

K-Number: K833072 · 1983-11-14

ApplicantTechnicon Instruments Corp.
Decision Date1983-11-14
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON RA-1000 SYS-ISE MODULE & 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 1983-11-14 under 510(k) number K833072. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON RA-1000 SYS-ISE MODULE &?

TECHNICON RA-1000 SYS-ISE MODULE & is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K833072.

When did TECHNICON RA-1000 SYS-ISE MODULE & receive FDA 510(k) clearance?

TECHNICON RA-1000 SYS-ISE MODULE & received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833072.

Who is the listed applicant for TECHNICON RA-1000 SYS-ISE MODULE &?

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 RA-1000 SYS-ISE MODULE &?

The FDA product code for TECHNICON RA-1000 SYS-ISE MODULE & is JGS.

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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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