Who is the manufacturer of CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

Valleylab, Inc. filed the 510(k) submission for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. (K931902).

What is the FDA product code for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

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

What is the regulatory pathway for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

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

Who can help prepare an FDA 510(k) submission like CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

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.

CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.

K931902 · Valleylab, Inc. · LFL · Sep 16, 1994 · SU

Device Facts

Record ID	K931902
Device Name	CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.
Applicant	Valleylab, Inc.
Product Code	LFL · SU
Decision Date	Sep 16, 1994
Decision	SESE
Submission Type	Traditional
Device Class	Class U

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