Cleared Traditional

K932235 - PRO. HI-LOW MAT TABLES #9610-9612 9620-9622
(FDA 510(k) Clearance)

K932235 · Bailey Mfg. Co. · Physical Medicine

Jul 1993

Decision

76d

Days

Class 1

Risk

K932235 is an FDA 510(k) clearance for the PRO. HI-LOW MAT TABLES #9610-9612 9620-9622, 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 review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number	K932235 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