RDH BANDAGE
K-Number: K002550 · 2000-12-20
Advertisement
Device Summary
Frequently Asked Questions
What is the RDH BANDAGE?
RDH BANDAGE is a medical device that received FDA 510(k) clearance on 2000-12-20. The listed applicant is Marine Polymer Technologies, Inc.. The 510(k) number is K002550.
When did RDH BANDAGE receive FDA 510(k) clearance?
RDH BANDAGE received FDA 510(k) clearance on 2000-12-20, under 510(k) number K002550.
Who is the listed applicant for RDH 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 RDH BANDAGE?
The FDA product code for RDH 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.
Advertisement