Cleared Traditional

THE PROTECTORS

K801312 · Cooper Medical Devices Corp. · General & Plastic Surgery

Jun 1980

Decision

14d

Days

—

Risk

About This 510(k) Submission

K801312 is an FDA 510(k) clearance for the THE PROTECTORS, submitted by Cooper Medical Devices Corp. (Mchenry, US). The FDA issued a Cleared decision on June 17, 1980, 14 days after receiving the submission on June 3, 1980. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number	K801312 FDA.gov
FDA Decision	Cleared SESE
Date Received	June 03, 1980
Decision Date	June 17, 1980
Days to Decision	14 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—