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FDA 510(k)

ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103

K-Number: K002909 · 2000-10-13

ApplicantAcrymed, Inc.
Decision Date2000-10-13
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 is the device name listed in this FDA 510(k) record. The listed applicant is Acrymed, Inc.. It received FDA 510(k) clearance on 2000-10-13 under 510(k) number K002909. 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 STRANDS MODEL A-020103?

ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 is a medical device that received FDA 510(k) clearance on 2000-10-13. The listed applicant is Acrymed, Inc.. The 510(k) number is K002909.

When did ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 receive FDA 510(k) clearance?

ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 received FDA 510(k) clearance on 2000-10-13, under 510(k) number K002909.

Who is the listed applicant for ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103?

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 STRANDS MODEL A-020103?

The FDA product code for ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 is FRO. This falls under the Anesthesiology category.

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Related Devices (Code: FRO)

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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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