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FDA 510(k)

ANEMIA I, II

K-Number: K911984 · 1991-06-13

ApplicantCiba Corning Diagnostics Corp.
Decision Date1991-06-13
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANEMIA I, II 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 1991-06-13 under 510(k) number K911984. 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 ANEMIA I, II?

ANEMIA I, II is a medical device that received FDA 510(k) clearance on 1991-06-13. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K911984.

When did ANEMIA I, II receive FDA 510(k) clearance?

ANEMIA I, II received FDA 510(k) clearance on 1991-06-13, under 510(k) number K911984.

Who is the listed applicant for ANEMIA I, II?

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 ANEMIA I, II?

The FDA product code for ANEMIA I, II is JJY.

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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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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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