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FDA 510(k)

CIBA CORNING MODEL 644

K-Number: K875098 · 1988-03-03

Decision Date1988-03-03
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CIBA CORNING MODEL 644 is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Corning Diagnostics Corp.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K875098. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIBA CORNING MODEL 644?

CIBA CORNING MODEL 644 is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K875098.

When did CIBA CORNING MODEL 644 receive FDA 510(k) clearance?

CIBA CORNING MODEL 644 received FDA 510(k) clearance on 1988-03-03, under 510(k) number K875098.

Who is the listed applicant for CIBA CORNING MODEL 644?

The FDA 510(k) record lists Ciba Corning Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIBA CORNING MODEL 644?

The FDA product code for CIBA CORNING MODEL 644 is JXR.

Related Clinical Trials

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.

Other records listing Ciba Corning Diagnostics 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: JXR)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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