Cleared Traditional

NUTROMAT

K831325 · Medlog GmbH Marketing Services · General & Plastic Surgery
Jun 1983
Decision
38d
Days
Class 1
Risk

About This 510(k) Submission

K831325 is an FDA 510(k) clearance for the NUTROMAT, a Chair, Surgical, Ac-powered (Class I — General Controls, product code GBB), submitted by Medlog GmbH Marketing Services (Mchenry, US). The FDA issued a Cleared decision on June 2, 1983, 38 days after receiving the submission on April 25, 1983. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.

Submission Details

510(k) Number K831325 FDA.gov
FDA Decision Cleared SESE
Date Received April 25, 1983
Decision Date June 02, 1983
Days to Decision 38 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary —

Device Classification

Product Code GBB — Chair, Surgical, Ac-powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4960