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FDA 510(k)

Curos Jet Disinfecting Cap

K-Number: K200299 · 2020-10-29

Applicant3M Company
Decision Date2020-10-29
Product CodeQBP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Curos Jet Disinfecting Cap is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 2020-10-29 under 510(k) number K200299. The device is classified under product code QBP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Curos Jet Disinfecting Cap?

Curos Jet Disinfecting Cap is a medical device that received FDA 510(k) clearance on 2020-10-29. The listed applicant is 3M Company. The 510(k) number is K200299.

When did Curos Jet Disinfecting Cap receive FDA 510(k) clearance?

Curos Jet Disinfecting Cap received FDA 510(k) clearance on 2020-10-29, under 510(k) number K200299.

Who is the listed applicant for Curos Jet Disinfecting Cap?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Curos Jet Disinfecting Cap?

The FDA product code for Curos Jet Disinfecting Cap is QBP.

Other records listing 3M Company 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 54 devices →

Related Devices (Code: QBP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.