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FDA 510(k)

HAEMOTRONIC BLOOD LINE SET

K-Number: K896407 · 1990-04-25

ApplicantHealthcare Suppliers, Inc.
Decision Date1990-04-25
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HAEMOTRONIC BLOOD LINE SET is the device name listed in this FDA 510(k) record. The listed applicant is Healthcare Suppliers, Inc.. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K896407. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMOTRONIC BLOOD LINE SET?

HAEMOTRONIC BLOOD LINE SET is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Healthcare Suppliers, Inc.. The 510(k) number is K896407.

When did HAEMOTRONIC BLOOD LINE SET receive FDA 510(k) clearance?

HAEMOTRONIC BLOOD LINE SET received FDA 510(k) clearance on 1990-04-25, under 510(k) number K896407.

Who is the listed applicant for HAEMOTRONIC BLOOD LINE SET?

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

What is the FDA product code for HAEMOTRONIC BLOOD LINE SET?

The FDA product code for HAEMOTRONIC BLOOD LINE SET is FJK.

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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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