Medline Vacu-line Suction Aspirator
K-Number: K203135 · 2021-05-04
Device Summary
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. The listed applicant is Medline Industries, Inc.. The 510(k) number is K203135.
When did Medline Vacu-line Suction Aspirator receive FDA 510(k) clearance?
Medline Vacu-line Suction Aspirator received FDA 510(k) clearance on 2021-05-04, under 510(k) number K203135.
Who is the listed applicant for Medline Vacu-line Suction Aspirator?
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 Vacu-line Suction Aspirator?
The FDA product code for Medline Vacu-line Suction Aspirator is BTA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medline Industries, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BTA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.