510(k) K931635

TREATMENT TABLES, MANUALLY ACTIVATED by Med Mart, Inc. — Product Code INW

K931635 is an FDA 510(k) premarket notification submitted by Med Mart, Inc. for the device "TREATMENT TABLES, MANUALLY ACTIVATED". The FDA issued a decision of Substantially Equivalent on July 21, 1993. The device falls under product code INW (Table, Mechanical), a Class I device regulated under 21 CFR 890.3750. Med Mart, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 21, 1993
Date Received
April 1, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Mechanical
Device Class
Class I
Regulation Number
890.3750
Review Panel
PM
Submission Type