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FDA 510(k)

ROBINSON MEDSURG QUICKSCREW RACK

K-Number: K093800 · 2010-06-16

ApplicantRobinson Medsurg, LLC
Decision Date2010-06-16
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ROBINSON MEDSURG QUICKSCREW RACK is the device name listed in this FDA 510(k) record. The listed applicant is Robinson Medsurg, LLC. It received FDA 510(k) clearance on 2010-06-16 under 510(k) number K093800. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROBINSON MEDSURG QUICKSCREW RACK?

ROBINSON MEDSURG QUICKSCREW RACK is a medical device that received FDA 510(k) clearance on 2010-06-16. The listed applicant is Robinson Medsurg, LLC. The 510(k) number is K093800.

When did ROBINSON MEDSURG QUICKSCREW RACK receive FDA 510(k) clearance?

ROBINSON MEDSURG QUICKSCREW RACK received FDA 510(k) clearance on 2010-06-16, under 510(k) number K093800.

Who is the listed applicant for ROBINSON MEDSURG QUICKSCREW RACK?

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

What is the FDA product code for ROBINSON MEDSURG QUICKSCREW RACK?

The FDA product code for ROBINSON MEDSURG QUICKSCREW RACK is KCT.

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Related Devices (Code: KCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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