510(k) K936303

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

K936303 is an FDA 510(k) premarket notification submitted by Tri W-G, Inc. for the device "TREATMENT TABLE MODIFICATION". The FDA issued a decision of Substantially Equivalent on March 18, 1994. 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
March 18, 1994
Date Received
November 19, 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