510(k) K931672
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