FDA 510(k)

MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK

K-Number: K875325 · 1988-02-18

Decision Date1988-02-18

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Schneider-Shilley (Usa). It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K875325. 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 MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK?

MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Schneider-Shilley (Usa). The 510(k) number is K875325.

When did MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK receive FDA 510(k) clearance?

MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK received FDA 510(k) clearance on 1988-02-18, under 510(k) number K875325.

Who is the listed applicant for MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK?

The FDA 510(k) record lists Schneider-Shilley (Usa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK?

The FDA product code for MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK 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.