Who is the manufacturer of ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103?

Acrymed, Inc. filed the 510(k) submission for ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 (K002909).

What is the FDA product code for ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103?

FRO. as a Class U device in the SU panel.

What is the regulatory pathway for ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103?

510(k) clearance (submission type: Special).

Who can help prepare an FDA 510(k) submission like ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103

K002909 · Acrymed, Inc. · FRO · Oct 13, 2000 · SU

Device Facts

Record ID	K002909
Device Name	ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103
Applicant	Acrymed, Inc.
Product Code	FRO · SU
Decision Date	Oct 13, 2000
Decision	SESE
Submission Type	Special
Device Class	Class U

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