Cleared Traditional

K932232 - PROFESSONAL HI-LOW WORK TABLE MODEL 3400
(FDA 510(k) Clearance)

K932232 · Bailey Mfg. Co. · Physical Medicine

Jul 1993

Decision

76d

Days

Class 1

Risk

K932232 is an FDA 510(k) clearance for the PROFESSONAL HI-LOW WORK TABLE MODEL 3400. This device is classified as a Table, Powered (Class I — General Controls, product code INQ).

Submitted by Bailey Mfg. Co. (Lodi, US). The FDA issued a Cleared decision on July 22, 1993, 76 days after receiving the submission on May 7, 1993.

This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number	K932232 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 07, 1993
Decision Date	July 22, 1993
Days to Decision	76 days
Submission Type	Traditional
Review Panel	Physical Medicine (PM)
Summary	Statement