FDA 510(k)

SCIMED 5, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS

K-Number: K934581 · 1994-03-31

Decision Date1994-03-31

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SCIMED 5, 7, AND 8 FRENCH 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 1994-03-31 under 510(k) number K934581. 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, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS?

SCIMED 5, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K934581.

When did SCIMED 5, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

SCIMED 5, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1994-03-31, under 510(k) number K934581.

Who is the listed applicant for SCIMED 5, 7, AND 8 FRENCH 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, 7, AND 8 FRENCH ANGIOGRAPHIC CATHETERS?

The FDA product code for SCIMED 5, 7, AND 8 FRENCH 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.