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FDA 510(k)

PADLOCK CLIP-12

K-Number: K120814 · 2012-09-06

ApplicantAponos Medical Corp.
Decision Date2012-09-06
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PADLOCK CLIP-12 is the device name listed in this FDA 510(k) record. The listed applicant is Aponos Medical Corp.. It received FDA 510(k) clearance on 2012-09-06 under 510(k) number K120814. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PADLOCK CLIP-12?

PADLOCK CLIP-12 is a medical device that received FDA 510(k) clearance on 2012-09-06. The listed applicant is Aponos Medical Corp.. The 510(k) number is K120814.

When did PADLOCK CLIP-12 receive FDA 510(k) clearance?

PADLOCK CLIP-12 received FDA 510(k) clearance on 2012-09-06, under 510(k) number K120814.

Who is the listed applicant for PADLOCK CLIP-12?

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

What is the FDA product code for PADLOCK CLIP-12?

The FDA product code for PADLOCK CLIP-12 is PKL.

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Official Source

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