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FDA 510(k)

ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER

K-Number: K892851 · 1989-09-26

ApplicantJohnson & Johnson Patient Care, Inc.
Decision Date1989-09-26
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Patient Care, Inc.. It received FDA 510(k) clearance on 1989-09-26 under 510(k) number K892851. 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 ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER?

ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Johnson & Johnson Patient Care, Inc.. The 510(k) number is K892851.

When did ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER receive FDA 510(k) clearance?

ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER received FDA 510(k) clearance on 1989-09-26, under 510(k) number K892851.

Who is the listed applicant for ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER?

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

What is the FDA product code for ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER?

The FDA product code for ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER is FRO. This falls under the Anesthesiology category.

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Other records listing Johnson & Johnson Patient Care, Inc. 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.

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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

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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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