Submission Details
| 510(k) Number | K093252 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 16, 2009 |
| Decision Date | December 17, 2009 |
| Days to Decision | 62 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Statement |
K093252 is an FDA 510(k) clearance for the FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER, a Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days (Class II — Special Controls, product code LJS), submitted by Footprint Medical, Inc. (San Antonio, US). The FDA issued a Cleared decision on December 17, 2009, 62 days after receiving the submission on October 16, 2009. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5970.
| 510(k) Number | K093252 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 16, 2009 |
| Decision Date | December 17, 2009 |
| Days to Decision | 62 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Statement |
| Product Code | LJS — Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 880.5970 |