510(k) K925594

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE by Tri W-G, Inc. — Product Code INQ

K925594 is an FDA 510(k) premarket notification submitted by Tri W-G, Inc. for the device "MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE". The FDA issued a decision of Substantially Equivalent on February 12, 1993. 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 12, 1993
Date Received
November 5, 1992
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