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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 the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2017-09-19 under 510(k) 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. The listed applicant is Medline Industries, Inc.. The 510(k) number is K170002.

When did Medline Blood Collection Set receive FDA 510(k) clearance?

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

Who is the listed applicant for Medline Blood Collection Set?

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

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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Related Devices (Code: 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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