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FDA 510(k)

COALIZA PROTEIN S-FREE

K-Number: K002467 · 2000-10-13

ApplicantInstrumentation Laboratory CO
Decision Date2000-10-13
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

COALIZA PROTEIN S-FREE is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2000-10-13 under 510(k) number K002467. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COALIZA PROTEIN S-FREE?

COALIZA PROTEIN S-FREE is a medical device that received FDA 510(k) clearance on 2000-10-13. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K002467.

When did COALIZA PROTEIN S-FREE receive FDA 510(k) clearance?

COALIZA PROTEIN S-FREE received FDA 510(k) clearance on 2000-10-13, under 510(k) number K002467.

Who is the listed applicant for COALIZA PROTEIN S-FREE?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COALIZA PROTEIN S-FREE?

The FDA product code for COALIZA PROTEIN S-FREE is GGP.

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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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