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FDA 510(k)

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER

K-Number: K870777 · 1987-03-13

Decision Date1987-03-13
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Kone Instruments, Inc.. It received FDA 510(k) clearance on 1987-03-13 under 510(k) number K870777. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER?

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Kone Instruments, Inc.. The 510(k) number is K870777.

When did PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER receive FDA 510(k) clearance?

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER received FDA 510(k) clearance on 1987-03-13, under 510(k) number K870777.

Who is the listed applicant for PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER?

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

What is the FDA product code for PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER?

The FDA product code for PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER is JJF.

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 Kone Instruments, 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.

View all 12 devices →

Related Devices (Code: JJF)

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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