MRDH BANDAGE
K-Number: K082703 · 2008-10-14
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Device Summary
Frequently Asked Questions
What is the MRDH BANDAGE?
MRDH BANDAGE is a medical device that received FDA 510(k) clearance on 2008-10-14. The listed applicant is Marine Polymer Technologies, Inc.. The 510(k) number is K082703.
When did MRDH BANDAGE receive FDA 510(k) clearance?
MRDH BANDAGE received FDA 510(k) clearance on 2008-10-14, under 510(k) number K082703.
Who is the listed applicant for MRDH BANDAGE?
The FDA 510(k) record lists Marine Polymer Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRDH BANDAGE?
The FDA product code for MRDH BANDAGE is KMF.
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 Marine Polymer Technologies, 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: KMF)
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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