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FDA 510(k)

ANTIBACTERIAL ADHESIVE BANDAGE

K-Number: K992817 · 1999-11-05

Decision Date1999-11-05
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

ANTIBACTERIAL ADHESIVE BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is William Feinstein & Associates, Inc.. It received FDA 510(k) clearance on 1999-11-05 under 510(k) number K992817. 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 ANTIBACTERIAL ADHESIVE BANDAGE?

ANTIBACTERIAL ADHESIVE BANDAGE is a medical device that received FDA 510(k) clearance on 1999-11-05. The listed applicant is William Feinstein & Associates, Inc.. The 510(k) number is K992817.

When did ANTIBACTERIAL ADHESIVE BANDAGE receive FDA 510(k) clearance?

ANTIBACTERIAL ADHESIVE BANDAGE received FDA 510(k) clearance on 1999-11-05, under 510(k) number K992817.

Who is the listed applicant for ANTIBACTERIAL ADHESIVE BANDAGE?

The FDA 510(k) record lists William Feinstein & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTIBACTERIAL ADHESIVE BANDAGE?

The FDA product code for ANTIBACTERIAL ADHESIVE BANDAGE 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.

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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