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FDA 510(k)

SENSILASE PAD-IQ

K-Number: K110438 · 2011-05-04

ApplicantVasamed, Inc.
Decision Date2011-05-04
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SENSILASE PAD-IQ is the device name listed in this FDA 510(k) record. The listed applicant is Vasamed, Inc.. It received FDA 510(k) clearance on 2011-05-04 under 510(k) number K110438. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSILASE PAD-IQ?

SENSILASE PAD-IQ is a medical device that received FDA 510(k) clearance on 2011-05-04. The listed applicant is Vasamed, Inc.. The 510(k) number is K110438.

When did SENSILASE PAD-IQ receive FDA 510(k) clearance?

SENSILASE PAD-IQ received FDA 510(k) clearance on 2011-05-04, under 510(k) number K110438.

Who is the listed applicant for SENSILASE PAD-IQ?

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

What is the FDA product code for SENSILASE PAD-IQ?

The FDA product code for SENSILASE PAD-IQ is DPW.

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Related Devices (Code: DPW)

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Official Source

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