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FDA 510(k)

Pelican Sling Retractor

K-Number: K153542 · 2016-09-07

ApplicantBeacon Surgical, Inc.
Decision Date2016-09-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Pelican Sling Retractor is a medical device manufactured by Beacon Surgical, Inc.. It received FDA 510(k) clearance on 2016-09-07 under approval number K153542. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pelican Sling Retractor?

Pelican Sling Retractor is a medical device that received FDA 510(k) clearance on 2016-09-07. It is manufactured by Beacon Surgical, Inc.. The 510(k) number is K153542.

When was Pelican Sling Retractor approved by the FDA?

Pelican Sling Retractor received FDA 510(k) clearance on 2016-09-07, under approval number K153542.

What company makes Pelican Sling Retractor?

Pelican Sling Retractor is manufactured by Beacon Surgical, Inc..

What is the FDA product code for Pelican Sling Retractor?

The FDA product code for Pelican Sling Retractor is GCJ.

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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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