Data / Medical devices / United States / Analytical Industries, Inc.
Analytical Industries, Inc.: FDA-registered device maker in Middleton, WI, United States, 3 510(k) clearances
Analytical Industries, Inc. is registered with the FDA (registration 2032134) in Middleton, WI, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated April 5, 2006. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2032134
- FEI number
- 3003098875
- Address
- 8605 Fairway Pl, Middleton, WI, United States, 53562
- Owner or operator
- Analytical Industries Inc (9021044)
- Roles
- Manufacturer
- First device listed
- October 22, 2007
- Registered through
- 2027
- Brand names listed
- AII 2000 % OXYGEN ANALYZER, AII 2000 SERIES O2 ANALYZER/MONITOR, Percent Oxygen Sensors
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Oxygen, Gaseous-Phase | CCL | 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 |
|---|---|---|---|---|---|---|
| April 5, 2006 | K053407 | OXYGEN ANALYZER, MODELS AII 20000A, AII 2000HC, AII 2000M | CCL | Substantially Equivalent | Analytical Industries, Inc. | accessdata.fda.gov |
| March 14, 2001 | K002382 | 'ALL 2000' % OXYGEN ANALYZER | CCL | Substantially Equivalent | Analytical Industries, Inc. | accessdata.fda.gov |
| October 18, 1995 | K952736 | PERCENT OXYGEN SENSOR | CCL | Substantially Equivalent | Analytical Industries, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 5, 2006. 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.