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FDA 510(k)

Removal System Large Bore 60 cc Syringe

K-Number: K233069 · 2024-03-26

ApplicantInari Medical, Inc.
Decision Date2024-03-26
Product CodePUR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Removal System Large Bore 60 cc Syringe is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2024-03-26 under approval number K233069. The device is classified under product code PUR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Removal System Large Bore 60 cc Syringe?

Removal System Large Bore 60 cc Syringe is a medical device that received FDA 510(k) clearance on 2024-03-26. It is manufactured by Inari Medical, Inc.. The 510(k) number is K233069.

When was Removal System Large Bore 60 cc Syringe approved by the FDA?

Removal System Large Bore 60 cc Syringe received FDA 510(k) clearance on 2024-03-26, under approval number K233069.

What company makes Removal System Large Bore 60 cc Syringe?

Removal System Large Bore 60 cc Syringe is manufactured by Inari Medical, Inc..

What is the FDA product code for Removal System Large Bore 60 cc Syringe?

The FDA product code for Removal System Large Bore 60 cc Syringe is PUR.

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Related PubMed Literature

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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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