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FDA 510(k)

CHLORIDE TEST

K-Number: K870630 · 1987-04-22

ApplicantSclavo, Inc.
Decision Date1987-04-22
Product CodeCHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHLORIDE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Sclavo, Inc.. It received FDA 510(k) clearance on 1987-04-22 under 510(k) number K870630. 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 TEST?

CHLORIDE TEST is a medical device that received FDA 510(k) clearance on 1987-04-22. The listed applicant is Sclavo, Inc.. The 510(k) number is K870630.

When did CHLORIDE TEST receive FDA 510(k) clearance?

CHLORIDE TEST received FDA 510(k) clearance on 1987-04-22, under 510(k) number K870630.

Who is the listed applicant for CHLORIDE TEST?

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

What is the FDA product code for CHLORIDE TEST?

The FDA product code for CHLORIDE TEST is CHJ.

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 Sclavo, Inc. 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.

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Related Devices (Code: CHJ)

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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