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FDA 510(k)

ULCER WOUND TRAY

K-Number: K922828 · 1992-09-28

ApplicantUlti-Med Intl., Inc.
Decision Date1992-09-28
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

ULCER WOUND TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 1992-09-28 under 510(k) number K922828. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ULCER WOUND TRAY?

ULCER WOUND TRAY is a medical device that received FDA 510(k) clearance on 1992-09-28. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K922828.

When did ULCER WOUND TRAY receive FDA 510(k) clearance?

ULCER WOUND TRAY received FDA 510(k) clearance on 1992-09-28, under 510(k) number K922828.

Who is the listed applicant for ULCER WOUND TRAY?

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

What is the FDA product code for ULCER WOUND TRAY?

The FDA product code for ULCER WOUND TRAY is KKX.

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Other records listing Ulti-Med Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KKX)

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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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