FDA 510(k)

SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS

K-Number: K964859 · 1997-02-10

Decision Date1997-02-10

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Scimed Life Systems, Inc.. It received FDA 510(k) clearance on 1997-02-10 under 510(k) number K964859. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS?

SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1997-02-10. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K964859.

When did SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1997-02-10, under 510(k) number K964859.

Who is the listed applicant for SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS?

The FDA 510(k) record lists Scimed Life Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS?

The FDA product code for SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS is DQO.

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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.