MICRO-VENT
K-Number: K864321 · 1987-01-07
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Device Summary
Frequently Asked Questions
What is the MICRO-VENT?
MICRO-VENT is a medical device that received FDA 510(k) clearance on 1987-01-07. The listed applicant is Core-Vent Corp.. The 510(k) number is K864321.
When did MICRO-VENT receive FDA 510(k) clearance?
MICRO-VENT received FDA 510(k) clearance on 1987-01-07, under 510(k) number K864321.
Who is the listed applicant for MICRO-VENT?
The FDA 510(k) record lists Core-Vent Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-VENT?
The FDA product code for MICRO-VENT is DZE.
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 Core-Vent 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: DZE)
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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