PROMOGRAN MATRIX WOUND DRESSING
K-Number: K014129 · 2002-02-14
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Device Summary
Frequently Asked Questions
What is the PROMOGRAN MATRIX WOUND DRESSING?
PROMOGRAN MATRIX WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2002-02-14. The listed applicant is Johnson & Johnson Medical, Ltd.. The 510(k) number is K014129.
When did PROMOGRAN MATRIX WOUND DRESSING receive FDA 510(k) clearance?
PROMOGRAN MATRIX WOUND DRESSING received FDA 510(k) clearance on 2002-02-14, under 510(k) number K014129.
Who is the listed applicant for PROMOGRAN MATRIX WOUND DRESSING?
The FDA 510(k) record lists Johnson & Johnson Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROMOGRAN MATRIX WOUND DRESSING?
The FDA product code for PROMOGRAN MATRIX WOUND DRESSING is KGN.
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 Johnson & Johnson Medical, Ltd. 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: KGN)
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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