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FDA 510(k)

SILVER FOAM WOUND DRESSING

K-Number: K914579 · 1992-02-21

Decision Date1992-02-21
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SILVER FOAM WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1992-02-21 under 510(k) number K914579. 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.

Frequently Asked Questions

What is the SILVER FOAM WOUND DRESSING?

SILVER FOAM WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Vitaphore Corp.. The 510(k) number is K914579.

When did SILVER FOAM WOUND DRESSING receive FDA 510(k) clearance?

SILVER FOAM WOUND DRESSING received FDA 510(k) clearance on 1992-02-21, under 510(k) number K914579.

Who is the listed applicant for SILVER FOAM WOUND DRESSING?

The FDA 510(k) record lists Vitaphore Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILVER FOAM WOUND DRESSING?

The FDA product code for SILVER FOAM WOUND DRESSING 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 Vitaphore Corp. 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

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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