FDA 510(k)

BLOOD DILUTION VIAL

K-Number: K844042 · 1984-10-23

Decision Date1984-10-23

Product CodeGKL

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

BLOOD DILUTION VIAL is the device name listed in this FDA 510(k) record. The listed applicant is American Scientific Products. It received FDA 510(k) clearance on 1984-10-23 under 510(k) number K844042. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD DILUTION VIAL?

BLOOD DILUTION VIAL is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is American Scientific Products. The 510(k) number is K844042.

When did BLOOD DILUTION VIAL receive FDA 510(k) clearance?

BLOOD DILUTION VIAL received FDA 510(k) clearance on 1984-10-23, under 510(k) number K844042.

Who is the listed applicant for BLOOD DILUTION VIAL?

The FDA 510(k) record lists American Scientific Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD DILUTION VIAL?

The FDA product code for BLOOD DILUTION VIAL is GKL.

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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.