510(k) K900644
K900644 is an FDA 510(k) premarket notification submitted by Infection Control Products, Inc. for the device "I.V. FREEDOM CLIP". The FDA issued a decision of Substantially Equivalent on March 9, 1990. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Infection Control Products, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 9, 1990
- Date Received
- February 9, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, Administration, Intravascular
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type