510(k) K933580

POWER WORK TABLE by Medical Device Inspection Co., Inc. — Product Code INQ

K933580 is an FDA 510(k) premarket notification submitted by Medical Device Inspection Co., Inc. for the device "POWER WORK TABLE". The FDA issued a decision of Substantially Equivalent on November 5, 1993. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Medical Device Inspection Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 5, 1993
Date Received
July 22, 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