Cleared Traditional

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM

K870718 · Span-America Medical Systems, Inc. · General Hospital
May 1987
Decision
76d
Days
—
Risk

About This 510(k) Submission

K870718 is an FDA 510(k) clearance for the AMERICAN ALCOHOL PREP PAD STERILE MEDIUM, a Pad, Alcohol, Device Disinfectant, submitted by Span-America Medical Systems, Inc. (Greenville, US). The FDA issued a Cleared decision on May 7, 1987, 76 days after receiving the submission on February 20, 1987. This device falls under the General Hospital review panel.

Submission Details

510(k) Number K870718 FDA.gov
FDA Decision Cleared SESE
Date Received February 20, 1987
Decision Date May 07, 1987
Days to Decision 76 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code LKB — Pad, Alcohol, Device Disinfectant
Device Class —