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FDA 510(k)

MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY

K-Number: K885188 · 1989-02-06

ApplicantQuinton, Inc.
Decision Date1989-02-06
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1989-02-06 under 510(k) number K885188. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY?

MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY is a medical device that received FDA 510(k) clearance on 1989-02-06. The listed applicant is Quinton, Inc.. The 510(k) number is K885188.

When did MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY receive FDA 510(k) clearance?

MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY received FDA 510(k) clearance on 1989-02-06, under 510(k) number K885188.

Who is the listed applicant for MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY?

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

What is the FDA product code for MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY?

The FDA product code for MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY is DWF.

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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.

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