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FDA 510(k)

VENTLAB VERIFY II

K-Number: K990098 · 1999-02-11

ApplicantVentlab Corp.
Decision Date1999-02-11
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLAB VERIFY II is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1999-02-11 under 510(k) number K990098. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTLAB VERIFY II?

VENTLAB VERIFY II is a medical device that received FDA 510(k) clearance on 1999-02-11. The listed applicant is Ventlab Corp.. The 510(k) number is K990098.

When did VENTLAB VERIFY II receive FDA 510(k) clearance?

VENTLAB VERIFY II received FDA 510(k) clearance on 1999-02-11, under 510(k) number K990098.

Who is the listed applicant for VENTLAB VERIFY II?

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

What is the FDA product code for VENTLAB VERIFY II?

The FDA product code for VENTLAB VERIFY II is BTR.

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Related Devices (Code: BTR)

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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