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FDA 510(k)

Medline Blood Collection Set

K-Number: K170002 · 2017-09-19

ApplicantMedline Industries, Inc.
Decision Date2017-09-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Medline Blood Collection Set is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2017-09-19 under approval number K170002. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Blood Collection Set?

Medline Blood Collection Set is a medical device that received FDA 510(k) clearance on 2017-09-19. It is manufactured by Medline Industries, Inc.. The 510(k) number is K170002.

When was Medline Blood Collection Set approved by the FDA?

Medline Blood Collection Set received FDA 510(k) clearance on 2017-09-19, under approval number K170002.

What company makes Medline Blood Collection Set?

Medline Blood Collection Set is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Blood Collection Set?

The FDA product code for Medline Blood Collection Set is FPA.

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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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