510(k) K932749

MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE by Med Mart, Inc. — Product Code INQ

K932749 is an FDA 510(k) premarket notification submitted by Med Mart, Inc. for the device "MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE". The FDA issued a decision of Substantially Equivalent on July 22, 1993. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Med Mart, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 22, 1993
Date Received
June 8, 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