FDA 510(k)

HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER

K-Number: K950344 · 1995-03-24

Decision Date1995-03-24

Product CodeFCM

Advisory CommitteeGU

DecisionUnknown

Device Summary

HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Acacia Laboratories, Inc.. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K950344. The device is classified under product code FCM. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER?

HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is Acacia Laboratories, Inc.. The 510(k) number is K950344.

When did HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER receive FDA 510(k) clearance?

HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER received FDA 510(k) clearance on 1995-03-24, under 510(k) number K950344.

Who is the listed applicant for HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER?

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

What is the FDA product code for HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER?

The FDA product code for HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER is FCM.

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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.