510(k) K831549
K831549 is an FDA 510(k) premarket notification submitted by Fred Sammons, Inc. for the device "ARM SLINGS". The FDA issued a decision of Substantially Equivalent on June 30, 1983. The device falls under product code ILI (Sling, Arm), a Class I device regulated under 21 CFR 890.3640. Fred Sammons, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 30, 1983
- Date Received
- May 12, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sling, Arm
- Device Class
- Class I
- Regulation Number
- 890.3640
- Review Panel
- PM
- Submission Type