510(k) K232300
K232300 is an FDA 510(k) premarket notification submitted by Elastimed , Ltd. for the device "ElastiMed SACS". The FDA issued a decision of Substantially Equivalent on Dec 22, 2023. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Elastimed , Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 22, 2023
- Date Received
- Aug 1, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sleeve, Limb, Compressible
- Device Class
- Class II
- Regulation Number
- 870.5800
- Review Panel
- CV
- Submission Type