510(k) K855054
K855054 is an FDA 510(k) premarket notification submitted by T.C. Retigo, Inc. for the device "THE WOOD PUMP 'OLE RED'". The FDA issued a decision of Substantially Equivalent on March 18, 1986. The device falls under product code KZD (Infusor, Pressure, For I.V. Bags), a Class I device regulated under 21 CFR 880.5420.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 18, 1986
- Date Received
- December 17, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Infusor, Pressure, For I.V. Bags
- Device Class
- Class I
- Regulation Number
- 880.5420
- Review Panel
- HO
- Submission Type