510(k) K932237

PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090 by Bailey Mfg. Co. — Product Code INQ

K932237 is an FDA 510(k) premarket notification submitted by Bailey Mfg. Co. for the device "PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090". The FDA issued a decision of Substantially Equivalent on July 22, 1993. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Bailey Mfg. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 22, 1993
Date Received
May 7, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Powered
Device Class
Class I
Regulation Number
890.3760
Review Panel
PM
Submission Type