Cleared Traditional

K922729 - SPARTA WET DRESSING, SODIUM CHLORIDE (FDA 510(k) Clearance)

Nov 1992
Decision
171d
Days
Risk

K922729 is an FDA 510(k) clearance for the SPARTA WET DRESSING, SODIUM CHLORIDE. This device is classified as a Dressing, Wound, Drug.

Submitted by Sparta Surgical Corp. (Hammonton, US). The FDA issued a Cleared decision on November 23, 1992, 171 days after receiving the submission on June 5, 1992.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K922729 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received June 05, 1992
Decision Date November 23, 1992
Days to Decision 171 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary

Device Classification

Product Code FRO — Dressing, Wound, Drug
Device Class

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