510(k) K903894
K903894 is an FDA 510(k) premarket notification submitted by Aci Medical, Inc. for the device "VENAPULSE MODELS VP-25 AND VP-50". The FDA issued a decision of Substantially Equivalent on April 3, 1991. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Aci Medical, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 3, 1991
- Date Received
- August 23, 1990
- 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