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FDA 510(k)

CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES

K-Number: K060927 · 2006-10-06

ApplicantCeres Medical Systems, LLC
Decision Date2006-10-06
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Ceres Medical Systems, LLC. It received FDA 510(k) clearance on 2006-10-06 under 510(k) number K060927. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES?

CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES is a medical device that received FDA 510(k) clearance on 2006-10-06. The listed applicant is Ceres Medical Systems, LLC. The 510(k) number is K060927.

When did CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES receive FDA 510(k) clearance?

CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES received FDA 510(k) clearance on 2006-10-06, under 510(k) number K060927.

Who is the listed applicant for CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES?

The FDA 510(k) record lists Ceres Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES?

The FDA product code for CERES PTA CATHETER MODELS PTA018,PTA035 VARIOUS SIZES is DQY.

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Related Devices (Code: DQY)

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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