510(k) K963526
K963526 is an FDA 510(k) premarket notification submitted by Alimed, Inc. for the device "STRAP WEDGE". The FDA issued a decision of Substantially Equivalent on October 28, 1996. The device falls under product code FMQ (Restraint, Protective), a Class I device regulated under 21 CFR 880.6760. Alimed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1996
- Date Received
- September 4, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Restraint, Protective
- Device Class
- Class I
- Regulation Number
- 880.6760
- Review Panel
- HO
- Submission Type