510(k) K001587 ยท CAZ Anesthesia Conduction Kit
19 GA PLASTIC REINFORCED EPIDURAL CATHETER
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Jul 12, 2000 |
| Received | May 23, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001587
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 13, 2026 | ARROW INTERNATIONAL, LLC Description/REF:
ACCESS TRAY/ASK-04001-SUH-S;
ACCESS TRAY/ASK-04001-VM1;
STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS;
STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS;
STIMUCATH SFTY KIT: Open, Classified |
CAZ | None listed |
| Sep 30, 2015 | Arrow International Inc Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes Terminated |
FOZ | None listed |
| Oct 22, 2014 | Arrow International Inc ASK-05501-AFH1, Lot Number 23F13K0969 Anesthesia Conduction Catheter, Epidural Anesthesia Kit Terminated |
CAZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.