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FDA 510(k)

REFLUX BED

K-Number: K896256 · 1989-11-08

ApplicantCozcon, Inc.
Decision Date1989-11-08
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REFLUX BED is the device name listed in this FDA 510(k) record. The listed applicant is Cozcon, Inc.. It received FDA 510(k) clearance on 1989-11-08 under 510(k) number K896256. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFLUX BED?

REFLUX BED is a medical device that received FDA 510(k) clearance on 1989-11-08. The listed applicant is Cozcon, Inc.. The 510(k) number is K896256.

When did REFLUX BED receive FDA 510(k) clearance?

REFLUX BED received FDA 510(k) clearance on 1989-11-08, under 510(k) number K896256.

Who is the listed applicant for REFLUX BED?

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

What is the FDA product code for REFLUX BED?

The FDA product code for REFLUX BED is INW.

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Related Devices (Code: INW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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