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FDA 510(k)

EOS IONIZED CALCIUM TEST CARD

K-Number: K896316 · 1990-02-13

Decision Date1990-02-13
Product CodeJFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EOS IONIZED CALCIUM TEST CARD is the device name listed in this FDA 510(k) record. The listed applicant is Eos Technology Corp.. It received FDA 510(k) clearance on 1990-02-13 under 510(k) number K896316. The device is classified under product code JFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EOS IONIZED CALCIUM TEST CARD?

EOS IONIZED CALCIUM TEST CARD is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is Eos Technology Corp.. The 510(k) number is K896316.

When did EOS IONIZED CALCIUM TEST CARD receive FDA 510(k) clearance?

EOS IONIZED CALCIUM TEST CARD received FDA 510(k) clearance on 1990-02-13, under 510(k) number K896316.

Who is the listed applicant for EOS IONIZED CALCIUM TEST CARD?

The FDA 510(k) record lists Eos Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EOS IONIZED CALCIUM TEST CARD?

The FDA product code for EOS IONIZED CALCIUM TEST CARD is JFP.

Related Clinical Trials

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.

Other records listing Eos Technology 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.

Related Devices (Code: JFP)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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