Hospitech Respiration
Lod Central IL, IL
HOSPITECH RESPIRATION appears in FDA device records in Lod Central IL, IL. FDA records list 6 510(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 6 510(k) clearances for Hospitech Respiration between 2010 and 2022. The busiest year on record is 2013, with 2. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 1 |
| 2013 | 2 |
| 2016 | 1 |
| 2018 | 1 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K221477 | AG100s | BSK | Substantially Equivalent | |
| K180991 | AG 100s | BSK | Substantially Equivalent | |
| K150157 | AnapnoGuard 100 Respiratory Guard System | BSK | Substantially Equivalent | |
| K131099 | AG MASS | JCX | Substantially Equivalent | |
| K122721 | AG GUFFILL | BSK | Substantially Equivalent | |
| K093126 | ANAPNOGUARD ENDOTRACHEAL TUBE | BTP | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3007682555 | 3007682555 | HOSPITECH RESPIRATION | 1 Galil St., Lod Central IL 701990 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