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FDA 510(k)

DECUBITUS CARE PAD

K-Number: K893969 · 1989-07-14

ApplicantGulftrade Exim, Inc.
Decision Date1989-07-14
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DECUBITUS CARE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Gulftrade Exim, Inc.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893969. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DECUBITUS CARE PAD?

DECUBITUS CARE PAD is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Gulftrade Exim, Inc.. The 510(k) number is K893969.

When did DECUBITUS CARE PAD receive FDA 510(k) clearance?

DECUBITUS CARE PAD received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893969.

Who is the listed applicant for DECUBITUS CARE PAD?

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

What is the FDA product code for DECUBITUS CARE PAD?

The FDA product code for DECUBITUS CARE PAD is FWZ.

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Related Devices (Code: FWZ)

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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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