DUMEX PAK-ITS WOVEN RIBBON PACKING
K-Number: K980791 · 1998-04-29
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Device Summary
Frequently Asked Questions
What is the DUMEX PAK-ITS WOVEN RIBBON PACKING?
DUMEX PAK-ITS WOVEN RIBBON PACKING is a medical device that received FDA 510(k) clearance on 1998-04-29. The listed applicant is Dumex Medical Surgical Products, Ltd.. The 510(k) number is K980791.
When did DUMEX PAK-ITS WOVEN RIBBON PACKING receive FDA 510(k) clearance?
DUMEX PAK-ITS WOVEN RIBBON PACKING received FDA 510(k) clearance on 1998-04-29, under 510(k) number K980791.
Who is the listed applicant for DUMEX PAK-ITS WOVEN RIBBON PACKING?
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 DUMEX PAK-ITS WOVEN RIBBON PACKING?
The FDA product code for DUMEX PAK-ITS WOVEN RIBBON PACKING 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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