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FDA 510(k)

MEDATRON CUVETTE DISC

K-Number: K873656 · 1987-12-14

ApplicantMedatron, Inc.
Decision Date1987-12-14
Product CodeJRI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDATRON CUVETTE DISC is the device name listed in this FDA 510(k) record. The listed applicant is Medatron, Inc.. It received FDA 510(k) clearance on 1987-12-14 under 510(k) number K873656. The device is classified under product code JRI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDATRON CUVETTE DISC?

MEDATRON CUVETTE DISC is a medical device that received FDA 510(k) clearance on 1987-12-14. The listed applicant is Medatron, Inc.. The 510(k) number is K873656.

When did MEDATRON CUVETTE DISC receive FDA 510(k) clearance?

MEDATRON CUVETTE DISC received FDA 510(k) clearance on 1987-12-14, under 510(k) number K873656.

Who is the listed applicant for MEDATRON CUVETTE DISC?

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

What is the FDA product code for MEDATRON CUVETTE DISC?

The FDA product code for MEDATRON CUVETTE DISC is JRI.

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Related Devices (Code: JRI)

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K780888THERMO SET ELECTRONIC TEM. CONTROLLERGilford Instrument Laboratories, Inc.K760769TEMPERATURE REGULATED FIVE CELL HOLDERSThe Perkin-Elmer Corp.K760197ACCUVETTE IICoulter Electronics, 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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