FDA 510(k)

SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS

K-Number: K961999 · 1996-11-19

Decision Date1996-11-19

Product CodeDYG

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Scimed, Inc.. It received FDA 510(k) clearance on 1996-11-19 under 510(k) number K961999. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS?

SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is Boston Scientific Scimed, Inc.. The 510(k) number is K961999.

When did SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS receive FDA 510(k) clearance?

SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS received FDA 510(k) clearance on 1996-11-19, under 510(k) number K961999.

Who is the listed applicant for SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS?

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

What is the FDA product code for SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS?

The FDA product code for SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS is DYG.

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Other records listing Boston Scientific Scimed, Inc. as applicant

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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.