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FDA 510(k)

CLIRPATH TURBO PERIPHERAL CATHETERS

K-Number: K060012 · 2006-09-29

ApplicantSpectranetics Corp.
Decision Date2006-09-29
Product CodePDU
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLIRPATH TURBO PERIPHERAL CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Spectranetics Corp.. It received FDA 510(k) clearance on 2006-09-29 under 510(k) number K060012. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLIRPATH TURBO PERIPHERAL CATHETERS?

CLIRPATH TURBO PERIPHERAL CATHETERS is a medical device that received FDA 510(k) clearance on 2006-09-29. The listed applicant is Spectranetics Corp.. The 510(k) number is K060012.

When did CLIRPATH TURBO PERIPHERAL CATHETERS receive FDA 510(k) clearance?

CLIRPATH TURBO PERIPHERAL CATHETERS received FDA 510(k) clearance on 2006-09-29, under 510(k) number K060012.

Who is the listed applicant for CLIRPATH TURBO PERIPHERAL CATHETERS?

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

What is the FDA product code for CLIRPATH TURBO PERIPHERAL CATHETERS?

The FDA product code for CLIRPATH TURBO PERIPHERAL CATHETERS is PDU.

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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.

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