Who is the manufacturer of SPARTA WET DRESSING, SODIUM CHLORIDE?

Sparta Surgical Corp. filed the 510(k) submission for SPARTA WET DRESSING, SODIUM CHLORIDE (K922729).

What is the FDA product code for SPARTA WET DRESSING, SODIUM CHLORIDE?

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

What is the regulatory pathway for SPARTA WET DRESSING, SODIUM CHLORIDE?

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

Who can help prepare an FDA 510(k) submission like SPARTA WET DRESSING, SODIUM CHLORIDE?

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.

SPARTA WET DRESSING, SODIUM CHLORIDE

K922729 · Sparta Surgical Corp. · FRO · Nov 23, 1992 · SU

Device Facts

Record ID	K922729
Device Name	SPARTA WET DRESSING, SODIUM CHLORIDE
Applicant	Sparta Surgical Corp.
Product Code	FRO · SU
Decision Date	Nov 23, 1992
Decision	SN
Submission Type	Traditional
Device Class	Class U

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