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FDA 510(k)

MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER

K-Number: K871388 · 1987-07-06

ApplicantBio-Rad
Decision Date1987-07-06
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1987-07-06 under 510(k) number K871388. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER?

MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER is a medical device that received FDA 510(k) clearance on 1987-07-06. The listed applicant is Bio-Rad. The 510(k) number is K871388.

When did MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER receive FDA 510(k) clearance?

MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER received FDA 510(k) clearance on 1987-07-06, under 510(k) number K871388.

Who is the listed applicant for MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER?

The FDA product code for MICROMAT MODEL 415 - BICHROMATIC FILTER PHOTOMETER is LCP.

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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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