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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 the device name listed in this FDA 510(k) record. The listed applicant is Inari Medical, Inc.. It received FDA 510(k) clearance on 2024-03-26 under 510(k) 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. The listed applicant is Inari Medical, Inc.. The 510(k) number is K233069.

When did Removal System Large Bore 60 cc Syringe receive FDA 510(k) clearance?

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

Who is the listed applicant for Removal System Large Bore 60 cc Syringe?

The FDA 510(k) record lists Inari Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: PUR)

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

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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