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FDA 510(k)

CALCIUM AND PH ELECTROLYTE ANALYZER

K-Number: K895397 · 1989-12-12

ApplicantIonetics, Inc.
Decision Date1989-12-12
Product CodeJFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALCIUM AND PH ELECTROLYTE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Ionetics, Inc.. It received FDA 510(k) clearance on 1989-12-12 under 510(k) number K895397. 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 CALCIUM AND PH ELECTROLYTE ANALYZER?

CALCIUM AND PH ELECTROLYTE ANALYZER is a medical device that received FDA 510(k) clearance on 1989-12-12. The listed applicant is Ionetics, Inc.. The 510(k) number is K895397.

When did CALCIUM AND PH ELECTROLYTE ANALYZER receive FDA 510(k) clearance?

CALCIUM AND PH ELECTROLYTE ANALYZER received FDA 510(k) clearance on 1989-12-12, under 510(k) number K895397.

Who is the listed applicant for CALCIUM AND PH ELECTROLYTE ANALYZER?

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

What is the FDA product code for CALCIUM AND PH ELECTROLYTE ANALYZER?

The FDA product code for CALCIUM AND PH ELECTROLYTE ANALYZER is JFP.

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Other records listing Ionetics, Inc. as applicant

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Related Devices (Code: 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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