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FDA 510(k)

JUPITER PTA CATHETERS (VARIOUS)

K-Number: K970299 · 1997-04-24

ApplicantCordis Corp.
Decision Date1997-04-24
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JUPITER PTA CATHETERS (VARIOUS) is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1997-04-24 under 510(k) number K970299. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JUPITER PTA CATHETERS (VARIOUS)?

JUPITER PTA CATHETERS (VARIOUS) is a medical device that received FDA 510(k) clearance on 1997-04-24. The listed applicant is Cordis Corp.. The 510(k) number is K970299.

When did JUPITER PTA CATHETERS (VARIOUS) receive FDA 510(k) clearance?

JUPITER PTA CATHETERS (VARIOUS) received FDA 510(k) clearance on 1997-04-24, under 510(k) number K970299.

Who is the listed applicant for JUPITER PTA CATHETERS (VARIOUS)?

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

What is the FDA product code for JUPITER PTA CATHETERS (VARIOUS)?

The FDA product code for JUPITER PTA CATHETERS (VARIOUS) is LIT.

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Related Devices (Code: LIT)

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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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