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FDA 510(k)

MP/S SINGLE WAVELENGTH MINI PHOTOMETER

K-Number: K920914 · 1992-03-23

ApplicantArtel, Inc.
Decision Date1992-03-23
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MP/S SINGLE WAVELENGTH 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 1992-03-23 under 510(k) number K920914. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MP/S SINGLE WAVELENGTH MINI PHOTOMETER?

MP/S SINGLE WAVELENGTH MINI PHOTOMETER is a medical device that received FDA 510(k) clearance on 1992-03-23. The listed applicant is Artel, Inc.. The 510(k) number is K920914.

When did MP/S SINGLE WAVELENGTH MINI PHOTOMETER receive FDA 510(k) clearance?

MP/S SINGLE WAVELENGTH MINI PHOTOMETER received FDA 510(k) clearance on 1992-03-23, under 510(k) number K920914.

Who is the listed applicant for MP/S SINGLE WAVELENGTH 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/S SINGLE WAVELENGTH MINI PHOTOMETER?

The FDA product code for MP/S SINGLE WAVELENGTH MINI PHOTOMETER is JJQ.

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 HEMOGLOBINOMETERK914809MP MINI PHOTOMETERK864542ARTEL DIFFERENTIAL PHOTOMETER

Related Devices (Code: JJQ)

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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