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FDA 510(k)

FLAME PHOTOMETER STANDARD #60083 160 NA/8K

K-Number: K871184 · 1987-05-28

Decision Date1987-05-28
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLAME PHOTOMETER STANDARD #60083 160 NA/8K is the device name listed in this FDA 510(k) record. The listed applicant is In Vitro Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-05-28 under 510(k) number K871184. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLAME PHOTOMETER STANDARD #60083 160 NA/8K?

FLAME PHOTOMETER STANDARD #60083 160 NA/8K is a medical device that received FDA 510(k) clearance on 1987-05-28. The listed applicant is In Vitro Diagnostics, Inc.. The 510(k) number is K871184.

When did FLAME PHOTOMETER STANDARD #60083 160 NA/8K receive FDA 510(k) clearance?

FLAME PHOTOMETER STANDARD #60083 160 NA/8K received FDA 510(k) clearance on 1987-05-28, under 510(k) number K871184.

Who is the listed applicant for FLAME PHOTOMETER STANDARD #60083 160 NA/8K?

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

What is the FDA product code for FLAME PHOTOMETER STANDARD #60083 160 NA/8K?

The FDA product code for FLAME PHOTOMETER STANDARD #60083 160 NA/8K is JIX.

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 In Vitro Diagnostics, 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 15 devices →

Related Devices (Code: JIX)

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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