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FDA 510(k)

MODEL 644 SWEAT DILUENT

K-Number: K935228 · 1994-08-01

ApplicantCiba Corning Diagnostics Corp.
Decision Date1994-08-01
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 644 SWEAT DILUENT 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 1994-08-01 under 510(k) number K935228. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 644 SWEAT DILUENT?

MODEL 644 SWEAT DILUENT is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K935228.

When did MODEL 644 SWEAT DILUENT receive FDA 510(k) clearance?

MODEL 644 SWEAT DILUENT received FDA 510(k) clearance on 1994-08-01, under 510(k) number K935228.

Who is the listed applicant for MODEL 644 SWEAT DILUENT?

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 MODEL 644 SWEAT DILUENT?

The FDA product code for MODEL 644 SWEAT DILUENT is CGZ.

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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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