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FDA 510(k)

FERTILITY PLUS 1, 2, 3

K-Number: K935219 · 1994-03-22

ApplicantCiba Corning Diagnostics Corp.
Decision Date1994-03-22
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FERTILITY PLUS 1, 2, 3 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 1994-03-22 under 510(k) number K935219. 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 FERTILITY PLUS 1, 2, 3?

FERTILITY PLUS 1, 2, 3 is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K935219.

When did FERTILITY PLUS 1, 2, 3 receive FDA 510(k) clearance?

FERTILITY PLUS 1, 2, 3 received FDA 510(k) clearance on 1994-03-22, under 510(k) number K935219.

Who is the listed applicant for FERTILITY PLUS 1, 2, 3?

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 FERTILITY PLUS 1, 2, 3?

The FDA product code for FERTILITY PLUS 1, 2, 3 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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Related Devices (Code: JJY)

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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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