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FDA 510(k)

SODIUM, POTASSIUM AND CHLORIDE PROCEDURE

K-Number: K861669 · 1986-05-27

ApplicantData Medical Associates, Inc.
Decision Date1986-05-27
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SODIUM, POTASSIUM AND CHLORIDE PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1986-05-27 under 510(k) number K861669. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SODIUM, POTASSIUM AND CHLORIDE PROCEDURE?

SODIUM, POTASSIUM AND CHLORIDE PROCEDURE is a medical device that received FDA 510(k) clearance on 1986-05-27. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K861669.

When did SODIUM, POTASSIUM AND CHLORIDE PROCEDURE receive FDA 510(k) clearance?

SODIUM, POTASSIUM AND CHLORIDE PROCEDURE received FDA 510(k) clearance on 1986-05-27, under 510(k) number K861669.

Who is the listed applicant for SODIUM, POTASSIUM AND CHLORIDE PROCEDURE?

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

What is the FDA product code for SODIUM, POTASSIUM AND CHLORIDE PROCEDURE?

The FDA product code for SODIUM, POTASSIUM AND CHLORIDE PROCEDURE is CGZ.

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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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