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FDA 510(k)

CUFF SENTRY

K-Number: K102674 · 2011-07-22

ApplicantVentlab Corp.
Decision Date2011-07-22
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CUFF SENTRY is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 2011-07-22 under 510(k) number K102674. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUFF SENTRY?

CUFF SENTRY is a medical device that received FDA 510(k) clearance on 2011-07-22. The listed applicant is Ventlab Corp.. The 510(k) number is K102674.

When did CUFF SENTRY receive FDA 510(k) clearance?

CUFF SENTRY received FDA 510(k) clearance on 2011-07-22, under 510(k) number K102674.

Who is the listed applicant for CUFF SENTRY?

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 CUFF SENTRY?

The FDA product code for CUFF SENTRY is BSK.

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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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