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FDA 510(k)

Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC)

K-Number: K240972 · 2024-06-07

Decision Date2024-06-07
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC) is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Service and Savings, Inc.. It received FDA 510(k) clearance on 2024-06-07 under 510(k) number K240972. 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 Medtronic Achieve Catheter Connecting Cable (2ACHC)?

Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC) is a medical device that received FDA 510(k) clearance on 2024-06-07. The listed applicant is Surgical Instrument Service and Savings, Inc.. The 510(k) number is K240972.

When did Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC) receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC) received FDA 510(k) clearance on 2024-06-07, under 510(k) number K240972.

Who is the listed applicant for Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC)?

The FDA 510(k) record lists Surgical Instrument Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC)?

The FDA product code for Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC) is NLH.

Other records listing Surgical Instrument Service and Savings, Inc. as applicant

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.

View all 23 devices →

Related Devices (Code: NLH)

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.

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.