On Site Gas Systems, Inc.
On Site Gas Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2010, with 1 FDA device recall on record.
Top product codes for On Site Gas Systems, Inc.
FDA recalls by On Site Gas Systems, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by On Site Gas Systems, Inc.
- K092636 — POGS, MODEL 65/130
- K063454 — POGS, MODEL 33C
- K041664 — PORTABLE OXYGEN GENERATION SYSTEM: POGS 33C
- K030920 — POGS 33
- K021581 — HEMOSORB
- K013390 — QUICKCLOT
- K021082 — ON SITE GAS SYSTEMS PORTABLE OXYGEN GENERATION SYSTEM-1.0 AND 5.0
- K020362 — P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM
- K014078 — ON SITE GAS SYSTEMS PORTABLE OXYGEN GENERATOR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.