FDA 510(k)

DELFLEX RIGID DRAIN CONTAINER

K-Number: K871155 · 1987-07-16

Decision Date1987-07-16

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DELFLEX RIGID DRAIN CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Delmed, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K871155. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELFLEX RIGID DRAIN CONTAINER?

DELFLEX RIGID DRAIN CONTAINER is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Delmed, Inc.. The 510(k) number is K871155.

When did DELFLEX RIGID DRAIN CONTAINER receive FDA 510(k) clearance?

DELFLEX RIGID DRAIN CONTAINER received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871155.

Who is the listed applicant for DELFLEX RIGID DRAIN CONTAINER?

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

What is the FDA product code for DELFLEX RIGID DRAIN CONTAINER?

The FDA product code for DELFLEX RIGID DRAIN CONTAINER is KDJ.

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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.