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FDA 510(k)

MICRO-VENT

K-Number: K864321 · 1987-01-07

Decision Date1987-01-07
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO-VENT is the device name listed in this FDA 510(k) record. The listed applicant is Core-Vent Corp.. It received FDA 510(k) clearance on 1987-01-07 under 510(k) number K864321. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 25 devices →

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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