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FDA 510(k)

SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER

K-Number: K921577 · 1992-10-16

ApplicantScimed Life Systems, Inc.
Decision Date1992-10-16
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER 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 1992-10-16 under 510(k) number K921577. 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 SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER?

SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER is a medical device that received FDA 510(k) clearance on 1992-10-16. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K921577.

When did SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER receive FDA 510(k) clearance?

SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER received FDA 510(k) clearance on 1992-10-16, under 510(k) number K921577.

Who is the listed applicant for SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER?

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 SIDEWINDER TUOHY-BORST Y-ADAPTER?

The FDA product code for SCIMED SIDEWINDER TUOHY-BORST Y-ADAPTER is LIT.

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Official Source

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