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FDA 510(k)

ICA1 IONIZED CALCIUM ANALYZER

K-Number: K801848 · 1980-10-31

ApplicantThe London Co.
Decision Date1980-10-31
Product CodeJFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ICA1 IONIZED CALCIUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is The London Co.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K801848. 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 ICA1 IONIZED CALCIUM ANALYZER?

ICA1 IONIZED CALCIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is The London Co.. The 510(k) number is K801848.

When did ICA1 IONIZED CALCIUM ANALYZER receive FDA 510(k) clearance?

ICA1 IONIZED CALCIUM ANALYZER received FDA 510(k) clearance on 1980-10-31, under 510(k) number K801848.

Who is the listed applicant for ICA1 IONIZED CALCIUM ANALYZER?

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

What is the FDA product code for ICA1 IONIZED CALCIUM ANALYZER?

The FDA product code for ICA1 IONIZED CALCIUM ANALYZER is JFP.

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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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