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FDA 510(k)

CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY

K-Number: K912158 · 1991-10-23

ApplicantMedical Device Inspection Co., Inc.
Decision Date1991-10-23
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1991-10-23 under 510(k) number K912158. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY?

CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K912158.

When did CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY receive FDA 510(k) clearance?

CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY received FDA 510(k) clearance on 1991-10-23, under 510(k) number K912158.

Who is the listed applicant for CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY?

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

What is the FDA product code for CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY?

The FDA product code for CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY is FOZ.

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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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