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FDA 510(k)

RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703

K-Number: K041123 · 2004-08-26

Decision Date2004-08-26
Product CodeDQO
Advisory CommitteeCV
DecisionUnknown

Device Summary

RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703 is the device name listed in this FDA 510(k) record. The listed applicant is Kerberos Proximal Solutions, Inc.. It received FDA 510(k) clearance on 2004-08-26 under 510(k) number K041123. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703?

RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703 is a medical device that received FDA 510(k) clearance on 2004-08-26. The listed applicant is Kerberos Proximal Solutions, Inc.. The 510(k) number is K041123.

When did RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703 receive FDA 510(k) clearance?

RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703 received FDA 510(k) clearance on 2004-08-26, under 510(k) number K041123.

Who is the listed applicant for RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703?

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

What is the FDA product code for RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703?

The FDA product code for RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703 is DQO.

Related Clinical Trials

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.

Other records listing Kerberos Proximal Solutions, 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.

Related Devices (Code: DQO)

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.

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