510(k) K830849

OB TILT by Lic-Orthion — Product Code INQ

K830849 is an FDA 510(k) premarket notification submitted by Lic-Orthion for the device "OB TILT". The FDA issued a decision of Substantially Equivalent on Apr 5, 1983. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Lic-Orthion has 16 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 5, 1983
Date Received
Mar 17, 1983
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
510(k) Exempt