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FDA 510(k)

DUMEX IODOFORM PACKING STRIP

K-Number: K990332 · 1999-04-14

Decision Date1999-04-14
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

DUMEX IODOFORM PACKING STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Dumex Medical Surgical Products, Ltd.. It received FDA 510(k) clearance on 1999-04-14 under 510(k) number K990332. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

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.

View all 13 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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