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FDA 510(k)

TECHNICON CHEMI

K-Number: K852565 · 1985-07-12

ApplicantTechnicon Instruments Corp.
Decision Date1985-07-12
Product CodeCGX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON CHEMI 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 1985-07-12 under 510(k) number K852565. The device is classified under product code CGX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON CHEMI?

TECHNICON CHEMI is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K852565.

When did TECHNICON CHEMI receive FDA 510(k) clearance?

TECHNICON CHEMI received FDA 510(k) clearance on 1985-07-12, under 510(k) number K852565.

Who is the listed applicant for TECHNICON CHEMI?

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 CHEMI?

The FDA product code for TECHNICON CHEMI is CGX.

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Other records listing Technicon Instruments Corp. 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.

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Related Devices (Code: CGX)

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.

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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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