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FDA 510(k)

AQUAPHOR R GAUZE

K-Number: K842967 · 1984-11-08

ApplicantBeiersdorf, Inc.
Decision Date1984-11-08
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

AQUAPHOR R GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K842967. 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 AQUAPHOR R GAUZE?

AQUAPHOR R GAUZE is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K842967.

When did AQUAPHOR R GAUZE receive FDA 510(k) clearance?

AQUAPHOR R GAUZE received FDA 510(k) clearance on 1984-11-08, under 510(k) number K842967.

Who is the listed applicant for AQUAPHOR R GAUZE?

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

What is the FDA product code for AQUAPHOR R GAUZE?

The FDA product code for AQUAPHOR R GAUZE is FRO. This falls under the Anesthesiology category.

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Other records listing Beiersdorf, Inc. as applicant

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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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