DUMEX IODOFORM PACKING STRIP
K-Number: K990332 · 1999-04-14
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Device Summary
Frequently Asked Questions
What is the DUMEX IODOFORM PACKING STRIP?
DUMEX IODOFORM PACKING STRIP is a medical device that received FDA 510(k) clearance on 1999-04-14. The listed applicant is Dumex Medical Surgical Products, Ltd.. The 510(k) number is K990332.
When did DUMEX IODOFORM PACKING STRIP receive FDA 510(k) clearance?
DUMEX IODOFORM PACKING STRIP received FDA 510(k) clearance on 1999-04-14, under 510(k) number K990332.
Who is the listed applicant for DUMEX IODOFORM PACKING STRIP?
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 IODOFORM PACKING STRIP?
The FDA product code for DUMEX IODOFORM PACKING STRIP is FRO. This falls under the Anesthesiology category.
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: FRO)
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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