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FDA 510(k)

ARTEL DIFFERENTIAL PHOTOMETER

K-Number: K864542 · 1987-02-06

ApplicantArtel, Inc.
Decision Date1987-02-06
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ARTEL DIFFERENTIAL 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 1987-02-06 under 510(k) number K864542. 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 ARTEL DIFFERENTIAL PHOTOMETER?

ARTEL DIFFERENTIAL PHOTOMETER is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Artel, Inc.. The 510(k) number is K864542.

When did ARTEL DIFFERENTIAL PHOTOMETER receive FDA 510(k) clearance?

ARTEL DIFFERENTIAL PHOTOMETER received FDA 510(k) clearance on 1987-02-06, under 510(k) number K864542.

Who is the listed applicant for ARTEL DIFFERENTIAL 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 ARTEL DIFFERENTIAL PHOTOMETER?

The FDA product code for ARTEL DIFFERENTIAL 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 HEMOGLOBINOMETERK920914MP/S SINGLE WAVELENGTH MINI PHOTOMETERK914809MP MINI 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

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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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