Upstream Peripheral Technologies Ltd.
Caesarea Central, IL
UPSTREAM PERIPHERAL TECHNOLOGIES LTD. appears in FDA device records in Caesarea Central, IL. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Upstream Peripheral Technologies Ltd. between 2012 and 2022. The busiest year on record is 2012, with 3. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2012 | 3 |
| 2019 | 1 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K211802 | GoBack Crossing Catheter | PDU | Substantially Equivalent | |
| K182937 | Upstream GoBack Crossing Catheter | DQY | Substantially Equivalent | |
| K120964 | UPSTREAM GR CATHETER | DQY | Substantially Equivalent | |
| K112887 | UPSTREAM NEEDLE HOLDER, UPSTREAM NEEDLE HOLDER WITH SHUT-OFF CONNECTOR | DYB | Substantially Equivalent | |
| K112886 | UPSTREAM SUPPORT CATHETER | DQY | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3009561706 | 3009561706 | UPSTREAM PERIPHERAL TECHNOLOGIES LTD. | 43 Haeshel st. ARAN building, Caesarea Central 3088900 IL | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain