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FDA 510(k)

MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY

K-Number: K072956 · 2007-11-07

ApplicantDerma Sciences, Inc.
Decision Date2007-11-07
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY is the device name listed in this FDA 510(k) record. The listed applicant is Derma Sciences, Inc.. It received FDA 510(k) clearance on 2007-11-07 under 510(k) number K072956. 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 MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY?

MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY is a medical device that received FDA 510(k) clearance on 2007-11-07. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K072956.

When did MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY receive FDA 510(k) clearance?

MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY received FDA 510(k) clearance on 2007-11-07, under 510(k) number K072956.

Who is the listed applicant for MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY?

The FDA 510(k) record lists Derma Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY?

The FDA product code for MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY is FRO. This falls under the Anesthesiology category.

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Other records listing Derma Sciences, Inc. as applicant

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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.

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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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