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FDA 510(k)

Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter

K-Number: K242225 · 2024-11-29

ApplicantSurgical Instrument Service and Savings, Inc.
Decision Date2024-11-29
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter is a medical device manufactured by Surgical Instrument Service and Savings, Inc.. It received FDA 510(k) clearance on 2024-11-29 under approval number K242225. The device is classified under product code NLH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter?

Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter is a medical device that received FDA 510(k) clearance on 2024-11-29. It is manufactured by Surgical Instrument Service and Savings, Inc.. The 510(k) number is K242225.

When was Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter approved by the FDA?

Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter received FDA 510(k) clearance on 2024-11-29, under approval number K242225.

What company makes Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter?

Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter is manufactured by Surgical Instrument Service and Savings, Inc..

What is the FDA product code for Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter?

The FDA product code for Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter is NLH.

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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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