FDA 510(k)

CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM

K-Number: K933151 · 1993-12-13

ApplicantContour Fabricators of Florida, Inc.

Decision Date1993-12-13

Product CodeFRG

Advisory CommitteeHO

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 1993-12-13 under 510(k) number K933151. The device is classified under product code FRG. It was reviewed by the HO 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 1993-12-13. The listed applicant is Contour Fabricators of Florida, Inc.. The 510(k) number is K933151.

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 1993-12-13, under 510(k) number K933151.

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 FRG.

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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.