Data / Medical devices / United States / Mission Systems Davenport Inc.
Mission Systems Davenport Inc.: FDA-registered device maker in Davenport, IA, United States, 1 510(k) clearance
Mission Systems Davenport Inc. is registered with the FDA (registration 3002840531) in Davenport, IA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2008. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002840531
- Address
- 2734 Hickory Grove Rd, Davenport, IA, United States, 52804
- Owner or operator
- Mission Systems Davenport Inc. (9047910)
- Roles
- Manufacturer
- First device listed
- October 27, 2014
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Medevac Use Oxygen Generator | OLF | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 22, 2008 | K082829 | AIRCRAFT MEDICAL OXYGEN GENERATION SYSTEM (AMOGS) | OLF | Substantially Equivalent | Carleton Life Support Systems, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| July 24, 2009 | 52766 | Not yet classified | Terminated | Cobham AMOGS Advanced Medical Oxygen Generating System, 70309-03900-101. Concentrator, Oxygen, Molecular Sieve, S/A P/N: 70309-03900-101, Mfg P/N 3261165-0101. The firm name on the label is Carleton Life Support Systems | The backup oxygen supply control valve on the oxygen concentrator could fail resulting in it sticking in the open or closed positions. | accessdata.fda.gov |
Updated September 16, 2009. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.