K900644 is an FDA 510(k) clearance for the I.V. FREEDOM CLIP. This device is classified as a Set, Administration, Intravascular (Class II - Special Controls, product code FPA).
Submitted by Infection Control Products, Inc. (Gardendale, US). The FDA issued a Cleared decision on March 9, 1990, 28 days after receiving the submission on February 9, 1990.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5440.
| 510(k) Number | K900644 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 09, 1990 |
| Decision Date | March 09, 1990 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | — |
| Product Code | FPA — Set, Administration, Intravascular |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 880.5440 |