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FDA 510(k)

CIBA CORNING 8-- SERIES CO-OXIMETER

K-Number: K946206 · 1995-01-30

ApplicantCiba Corning Diagnostics Corp.
Decision Date1995-01-30
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CIBA CORNING 8-- SERIES CO-OXIMETER 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 1995-01-30 under 510(k) number K946206. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIBA CORNING 8-- SERIES CO-OXIMETER?

CIBA CORNING 8-- SERIES CO-OXIMETER is a medical device that received FDA 510(k) clearance on 1995-01-30. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K946206.

When did CIBA CORNING 8-- SERIES CO-OXIMETER receive FDA 510(k) clearance?

CIBA CORNING 8-- SERIES CO-OXIMETER received FDA 510(k) clearance on 1995-01-30, under 510(k) number K946206.

Who is the listed applicant for CIBA CORNING 8-- SERIES CO-OXIMETER?

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 8-- SERIES CO-OXIMETER?

The FDA product code for CIBA CORNING 8-- SERIES CO-OXIMETER is CHL.

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Other records listing Ciba Corning Diagnostics Corp. as applicant

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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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