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FDA 510(k)

MULTIQUAL UNASSAYED PRODUCTS

K-Number: K923632 · 1992-10-13

ApplicantCiba Corning Diagnostics Corp.
Decision Date1992-10-13
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTIQUAL UNASSAYED PRODUCTS 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 1992-10-13 under 510(k) number K923632. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIQUAL UNASSAYED PRODUCTS?

MULTIQUAL UNASSAYED PRODUCTS is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K923632.

When did MULTIQUAL UNASSAYED PRODUCTS receive FDA 510(k) clearance?

MULTIQUAL UNASSAYED PRODUCTS received FDA 510(k) clearance on 1992-10-13, under 510(k) number K923632.

Who is the listed applicant for MULTIQUAL UNASSAYED PRODUCTS?

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 MULTIQUAL UNASSAYED PRODUCTS?

The FDA product code for MULTIQUAL UNASSAYED PRODUCTS is JJY.

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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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