510(k) K930262

TREATMENT TABLE, MODEL #825-100 by Biodan Medical Systems, Ltd. — Product Code INO

K930262 is an FDA 510(k) premarket notification submitted by Biodan Medical Systems, Ltd. for the device "TREATMENT TABLE, MODEL #825-100". The FDA issued a decision of Substantially Equivalent on March 29, 1993. The device falls under product code INO (Chair, Positioning, Electric), a Class II device regulated under 21 CFR 890.3110. Biodan Medical Systems, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 1993
Date Received
January 19, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Positioning, Electric
Device Class
Class II
Regulation Number
890.3110
Review Panel
PM
Submission Type