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FDA 510(k)

CIRCUMAURAL ADHESIVE REPLACEMENT

K-Number: K111555 · 2011-07-25

ApplicantR & D Medical Products, Inc.
Decision Date2011-07-25
Product CodeGWJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CIRCUMAURAL ADHESIVE REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is R & D Medical Products, Inc.. It received FDA 510(k) clearance on 2011-07-25 under 510(k) number K111555. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUMAURAL ADHESIVE REPLACEMENT?

CIRCUMAURAL ADHESIVE REPLACEMENT is a medical device that received FDA 510(k) clearance on 2011-07-25. The listed applicant is R & D Medical Products, Inc.. The 510(k) number is K111555.

When did CIRCUMAURAL ADHESIVE REPLACEMENT receive FDA 510(k) clearance?

CIRCUMAURAL ADHESIVE REPLACEMENT received FDA 510(k) clearance on 2011-07-25, under 510(k) number K111555.

Who is the listed applicant for CIRCUMAURAL ADHESIVE REPLACEMENT?

The FDA 510(k) record lists R & D Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIRCUMAURAL ADHESIVE REPLACEMENT?

The FDA product code for CIRCUMAURAL ADHESIVE REPLACEMENT is GWJ.

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Other records listing R & D Medical Products, Inc. as applicant

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Related Devices (Code: GWJ)

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Official Source

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