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FDA 510(k)

CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM

K-Number: K934072 · 1994-09-08

ApplicantContour Fabricators of Florida, Inc.
Decision Date1994-09-08
Product CodeKNY
Advisory CommitteeGU
DecisionUnknown

Device Summary

CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators of Florida, Inc.. It received FDA 510(k) clearance on 1994-09-08 under 510(k) number K934072. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM?

CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-08. The listed applicant is Contour Fabricators of Florida, Inc.. The 510(k) number is K934072.

When did CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM receive FDA 510(k) clearance?

CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM received FDA 510(k) clearance on 1994-09-08, under 510(k) number K934072.

Who is the listed applicant for CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM?

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

What is the FDA product code for CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM?

The FDA product code for CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM is KNY.

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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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