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FDA 510(k)

KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM

K-Number: K050130 · 2005-05-13

ApplicantKerberos Proximal Solutions, Inc.
Decision Date2005-05-13
Product CodeQEZ
Advisory CommitteeCV
DecisionUnknown

Device Summary

KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM 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 2005-05-13 under 510(k) number K050130. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM?

KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-13. The listed applicant is Kerberos Proximal Solutions, Inc.. The 510(k) number is K050130.

When did KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM receive FDA 510(k) clearance?

KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM received FDA 510(k) clearance on 2005-05-13, under 510(k) number K050130.

Who is the listed applicant for KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM?

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 KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM?

The FDA product code for KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM is QEZ.

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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.

K062275RINSPIRATION CATHETER SYSTEM, MODELS 50135, 550135, P7065, P70135K041123RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703K041151KERBEROS OCCLUDING GUIDE CATHETER AND ACCESSORIESK041291RINSPIRATION SYSTEM

Related Devices (Code: QEZ)

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

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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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