K981035 is an FDA 510(k) clearance for the PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES. This device is classified as a Tubes, Vials, Systems, Serum Separators, Blood Collection (Class II - Special Controls, product code JKA).
Submitted by Sims Portex, Inc. (Keene, US). The FDA issued a Cleared decision on April 21, 1998, 33 days after receiving the submission on March 19, 1998.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1675.
| 510(k) Number | K981035 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 19, 1998 |
| Decision Date | April 21, 1998 |
| Days to Decision | 33 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JKA — Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1675 |