WOUND DRESSING KIT
K-Number: K923905 · 1993-07-02
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Device Summary
Frequently Asked Questions
What is the WOUND DRESSING KIT?
WOUND DRESSING KIT is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Kit Pak, Inc.. The 510(k) number is K923905.
When did WOUND DRESSING KIT receive FDA 510(k) clearance?
WOUND DRESSING KIT received FDA 510(k) clearance on 1993-07-02, under 510(k) number K923905.
Who is the listed applicant for WOUND DRESSING KIT?
The FDA 510(k) record lists Kit Pak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WOUND DRESSING KIT?
The FDA product code for WOUND DRESSING KIT is MCY.
Related Clinical Trials
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.
Other records listing Kit Pak, 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.
Related Devices (Code: MCY)
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.
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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