VIAL VENT FILTER
K-Number: K852467 · 1985-10-17
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Device Summary
Frequently Asked Questions
What is the VIAL VENT FILTER?
VIAL VENT FILTER is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K852467.
When did VIAL VENT FILTER receive FDA 510(k) clearance?
VIAL VENT FILTER received FDA 510(k) clearance on 1985-10-17, under 510(k) number K852467.
Who is the listed applicant for VIAL VENT FILTER?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIAL VENT FILTER?
The FDA product code for VIAL VENT FILTER is LHI.
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 Baxter Healthcare Corp 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: LHI)
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.
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