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FDA 510(k)

CHLORIDE PROCEDURE, TEKPOINT DIRECT

K-Number: K770450 · 1977-05-03

ApplicantIcn Pharmaceuticals, Inc.
Decision Date1977-05-03
Product CodeCHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHLORIDE PROCEDURE, TEKPOINT DIRECT is the device name listed in this FDA 510(k) record. The listed applicant is Icn Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1977-05-03 under 510(k) number K770450. The device is classified under product code CHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLORIDE PROCEDURE, TEKPOINT DIRECT?

CHLORIDE PROCEDURE, TEKPOINT DIRECT is a medical device that received FDA 510(k) clearance on 1977-05-03. The listed applicant is Icn Pharmaceuticals, Inc.. The 510(k) number is K770450.

When did CHLORIDE PROCEDURE, TEKPOINT DIRECT receive FDA 510(k) clearance?

CHLORIDE PROCEDURE, TEKPOINT DIRECT received FDA 510(k) clearance on 1977-05-03, under 510(k) number K770450.

Who is the listed applicant for CHLORIDE PROCEDURE, TEKPOINT DIRECT?

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

What is the FDA product code for CHLORIDE PROCEDURE, TEKPOINT DIRECT?

The FDA product code for CHLORIDE PROCEDURE, TEKPOINT DIRECT is CHJ.

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Related Devices (Code: CHJ)

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K010670PICCOLO CHLORIDE TEST SYSTEMAbaxis, Inc.K945408340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZERCatachem, Inc.K943006CHLORIDE QVETPrisma SystemsK934136OLYMPUS CHLORIDE REAGENT, MODIFICATIONOlympus Corp.K932528OLYMPUS CHLORID REAGENT, MODIFIEDOlympus Corp.K925338OLYMPUS CHLORIDE REAGENTOlympus Corp.

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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