510(k) K960196

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 by Tri W-G, Inc. — Product Code INQ

K960196 is an FDA 510(k) premarket notification submitted by Tri W-G, Inc. for the device "TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777". The FDA issued a decision of Substantially Equivalent on February 7, 1996. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Tri W-G, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1996
Date Received
January 16, 1996
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