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FDA 510(k)

Medline Vacu-line Suction Aspirator

K-Number: K203135 · 2021-05-04

ApplicantMedline Industries, Inc.
Decision Date2021-05-04
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline Vacu-line Suction Aspirator is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2021-05-04 under approval number K203135. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Vacu-line Suction Aspirator?

Medline Vacu-line Suction Aspirator is a medical device that received FDA 510(k) clearance on 2021-05-04. It is manufactured by Medline Industries, Inc.. The 510(k) number is K203135.

When was Medline Vacu-line Suction Aspirator approved by the FDA?

Medline Vacu-line Suction Aspirator received FDA 510(k) clearance on 2021-05-04, under approval number K203135.

What company makes Medline Vacu-line Suction Aspirator?

Medline Vacu-line Suction Aspirator is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Vacu-line Suction Aspirator?

The FDA product code for Medline Vacu-line Suction Aspirator is BTA.

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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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