510(k) K912010
K912010 is an FDA 510(k) premarket notification submitted by Dina - Industria, Comercio E Exportacao , Ltd. for the device "I.V. SKY-HOOK". The FDA issued a decision of Substantially Equivalent on August 19, 1991. The device falls under product code FOX (Stand, Infusion), a Class I device regulated under 21 CFR 880.6990.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 1991
- Date Received
- May 6, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stand, Infusion
- Device Class
- Class I
- Regulation Number
- 880.6990
- Review Panel
- HO
- Submission Type