Cleared Traditional

DR7700 OPERATING TABLE

K864325 · Koken Mfg Company, Inc. · General & Plastic Surgery
Nov 1986
Decision
16d
Days
Class 1
Risk

About This 510(k) Submission

K864325 is an FDA 510(k) clearance for the DR7700 OPERATING TABLE, a Table, Operating-room, Ac-powered (Class I — General Controls, product code FQO), submitted by Koken Mfg Company, Inc. (St. Louis, US). The FDA issued a Cleared decision on November 19, 1986, 16 days after receiving the submission on November 3, 1986. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.

Submission Details

510(k) Number K864325 FDA.gov
FDA Decision Cleared SESE
Date Received November 03, 1986
Decision Date November 19, 1986
Days to Decision 16 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary

Device Classification

Product Code FQO — Table, Operating-room, Ac-powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4960