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FDA 510(k)

SureForm 45 Curved Tip, SureForm 45 Gray Reload

K-Number: K190999 · 2019-07-12

Decision Date2019-07-12
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SureForm 45 Curved Tip, SureForm 45 Gray Reload is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2019-07-12 under approval number K190999. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SureForm 45 Curved Tip, SureForm 45 Gray Reload?

SureForm 45 Curved Tip, SureForm 45 Gray Reload is a medical device that received FDA 510(k) clearance on 2019-07-12. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K190999.

When was SureForm 45 Curved Tip, SureForm 45 Gray Reload approved by the FDA?

SureForm 45 Curved Tip, SureForm 45 Gray Reload received FDA 510(k) clearance on 2019-07-12, under approval number K190999.

What company makes SureForm 45 Curved Tip, SureForm 45 Gray Reload?

SureForm 45 Curved Tip, SureForm 45 Gray Reload is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for SureForm 45 Curved Tip, SureForm 45 Gray Reload?

The FDA product code for SureForm 45 Curved Tip, SureForm 45 Gray Reload is NAY.

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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.