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FDA 510(k)

WOUND PROTECTOR/RETRACTOR

K-Number: K020435 · 2002-04-15

ApplicantApplied Medical Resources Corp.
Decision Date2002-04-15
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WOUND PROTECTOR/RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2002-04-15 under 510(k) number K020435. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND PROTECTOR/RETRACTOR?

WOUND PROTECTOR/RETRACTOR is a medical device that received FDA 510(k) clearance on 2002-04-15. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K020435.

When did WOUND PROTECTOR/RETRACTOR receive FDA 510(k) clearance?

WOUND PROTECTOR/RETRACTOR received FDA 510(k) clearance on 2002-04-15, under 510(k) number K020435.

Who is the listed applicant for WOUND PROTECTOR/RETRACTOR?

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

What is the FDA product code for WOUND PROTECTOR/RETRACTOR?

The FDA product code for WOUND PROTECTOR/RETRACTOR is KKX.

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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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