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FDA 510(k)

ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006

K-Number: K061232 · 2006-10-06

ApplicantAcrymed, Inc.
Decision Date2006-10-06
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 is the device name listed in this FDA 510(k) record. The listed applicant is Acrymed, Inc.. It received FDA 510(k) clearance on 2006-10-06 under 510(k) number K061232. 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 ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006?

ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 is a medical device that received FDA 510(k) clearance on 2006-10-06. The listed applicant is Acrymed, Inc.. The 510(k) number is K061232.

When did ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 receive FDA 510(k) clearance?

ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 received FDA 510(k) clearance on 2006-10-06, under 510(k) number K061232.

Who is the listed applicant for ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006?

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

What is the FDA product code for ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006?

The FDA product code for ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 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 Acrymed, 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 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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