510(k) K910838

TREATMENT TABLE by Tri W-G, Inc. — Product Code IXR

K910838 is an FDA 510(k) premarket notification submitted by Tri W-G, Inc. for the device "TREATMENT TABLE". The FDA issued a decision of Substantially Equivalent on August 7, 1991. The device falls under product code IXR (Table, Radiographic, Tilting), a Class II device regulated under 21 CFR 892.1980. Tri W-G, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1991
Date Received
February 27, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Radiographic, Tilting
Device Class
Class II
Regulation Number
892.1980
Review Panel
RA
Submission Type