Mespere Lifesciences Inc.
Waterloo Ontario, CA
MESPERE LIFESCIENCES INC. appears in FDA device records in Waterloo Ontario, CA. FDA records list 3 510(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 3 510(k) clearances for Mespere Lifesciences Inc. between 2013 and 2018. The busiest year on record is 2013, with 1. The most recent is 2018, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2013 | 1 |
| 2015 | 1 |
| 2018 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K182242 | VO200 – NeurOs Cerebral Oximetry System | QEM | Substantially Equivalent | |
| K151776 | Central Venous Pressure System | PFA | Substantially Equivalent | |
| K131085 | CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000 | PFA | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3010521858 | 3010521858 | MESPERE LIFESCIENCES INC. | 180 Columbia Street West, Units 1A & 1B, Waterloo Ontario N2L 3L3 CA | 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