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FDA 510(k)

VACVENT

K-Number: K931873 · 1993-12-30

ApplicantSteven Frank Mercereau
Decision Date1993-12-30
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

VACVENT is the device name listed in this FDA 510(k) record. The listed applicant is Steven Frank Mercereau. It received FDA 510(k) clearance on 1993-12-30 under 510(k) number K931873. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VACVENT?

VACVENT is a medical device that received FDA 510(k) clearance on 1993-12-30. The listed applicant is Steven Frank Mercereau. The 510(k) number is K931873.

When did VACVENT receive FDA 510(k) clearance?

VACVENT received FDA 510(k) clearance on 1993-12-30, under 510(k) number K931873.

Who is the listed applicant for VACVENT?

The FDA 510(k) record lists Steven Frank Mercereau as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACVENT?

The FDA product code for VACVENT is CBT.

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Related Devices (Code: CBT)

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.

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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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