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FDA 510(k)

AUTOTECHNICON V TISSUE PROCESS SYS

K-Number: K834599 · 1984-02-04

ApplicantTechnicon Instruments Corp.
Decision Date1984-02-04
Product CodeIEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

AUTOTECHNICON V TISSUE PROCESS SYS 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 1984-02-04 under 510(k) number K834599. The device is classified under product code IEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOTECHNICON V TISSUE PROCESS SYS?

AUTOTECHNICON V TISSUE PROCESS SYS is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K834599.

When did AUTOTECHNICON V TISSUE PROCESS SYS receive FDA 510(k) clearance?

AUTOTECHNICON V TISSUE PROCESS SYS received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834599.

Who is the listed applicant for AUTOTECHNICON V TISSUE PROCESS SYS?

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 AUTOTECHNICON V TISSUE PROCESS SYS?

The FDA product code for AUTOTECHNICON V TISSUE PROCESS SYS is IEO.

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Other records listing Technicon Instruments Corp. as applicant

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Related Devices (Code: IEO)

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.

K924590MICROWAVE AUTOMATED TISSUE PROCESSORInnovative Medical Systems, Inc.K883599LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)Innovative Medical Systems, Inc.K881165SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSORSakura Finetek U.S.A., Inc.K853938LX 300 TISSUE PROCESSORInnovative Medical Systems, Inc.K851054LX120 TISSUE PROCESSORInnovative Medical Systems, Inc.K843506LKB 2189 ULTROPROCESSORLkb Instruments, 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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