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FDA 510(k)

MP MINI PHOTOMETER

K-Number: K914809 · 1992-01-27

ApplicantArtel, Inc.
Decision Date1992-01-27
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MP MINI PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Artel, Inc.. It received FDA 510(k) clearance on 1992-01-27 under 510(k) number K914809. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MP MINI PHOTOMETER?

MP MINI PHOTOMETER is a medical device that received FDA 510(k) clearance on 1992-01-27. The listed applicant is Artel, Inc.. The 510(k) number is K914809.

When did MP MINI PHOTOMETER receive FDA 510(k) clearance?

MP MINI PHOTOMETER received FDA 510(k) clearance on 1992-01-27, under 510(k) number K914809.

Who is the listed applicant for MP MINI PHOTOMETER?

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

What is the FDA product code for MP MINI PHOTOMETER?

The FDA product code for MP MINI PHOTOMETER is JJX.

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.

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Other records listing Artel, 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.

K933836HBM HEMOGLOBINOMETERK920914MP/S SINGLE WAVELENGTH MINI PHOTOMETERK864542ARTEL DIFFERENTIAL PHOTOMETER

Related Devices (Code: JJX)

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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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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