510(k) K931672

CARAPACE STERILE CAST PADDING by Carapace, Inc. — Product Code LGF

K931672 is an FDA 510(k) premarket notification submitted by Carapace, Inc. for the device "CARAPACE STERILE CAST PADDING". The FDA issued a decision of Substantially Equivalent on December 15, 1993. The device falls under product code LGF (Component, Cast), a Class I device regulated under 21 CFR 888.5940. Carapace, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 15, 1993
Date Received
April 6, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Component, Cast
Device Class
Class I
Regulation Number
888.5940
Review Panel
OR
Submission Type