DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE)
K-Number: K945830 · 1995-01-11
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Device Summary
Frequently Asked Questions
What is the DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE)?
DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE) is a medical device that received FDA 510(k) clearance on 1995-01-11. The listed applicant is Dumex Medical Surgical Products, Ltd.. The 510(k) number is K945830.
When did DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE) receive FDA 510(k) clearance?
DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE) received FDA 510(k) clearance on 1995-01-11, under 510(k) number K945830.
Who is the listed applicant for DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE)?
The FDA 510(k) record lists Dumex Medical Surgical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE)?
The FDA product code for DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE) is EFQ.
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 Dumex Medical Surgical Products, 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: EFQ)
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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