Warren E. Collins, Inc.
United StatesFDA applicant, unverified
- Devices
- 14
What Warren E. Collins, Inc. makes
Warren E. Collins, Inc. manufactures respiratory diagnostic devices, including systems for measuring residual lung volume, computerized pulmonary function testing, and body plethysmography. Their portfolio includes modular pulmonary function testers, pneumotachometers, and specialized components like thermoplastic rubber shells for medical equipment. Products like the Collins DS and Spira Elektro 2 are designed for clinical assessment of lung function, while the Pedalmate 2 and Eagle II focus on peripheral vascular testing.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) database. These products are intended for use in clinical settings to evaluate respiratory and circulatory function. The manufacturer operates from the United States, adhering to applicable U.S. medical device regulations.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Warren E. Collins, Inc. have in the registry?
The registry currently lists 14 devices for Warren E. Collins, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Warren E. Collins, Inc.'s devices?
Among its 14 most recently registered devices, Warren E. Collins, Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do Warren E. Collins, Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Warren E. Collins, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Warren E. Collins, Inc. in the registry?
The most recently registered devices listed for Warren E. Collins, Inc. include RS-RESIDUAL VOLUME SYSTEM, PULMONARY FUNCTION TESTER, COMPUTERIZED, COLLINS DS and THE SPIRA ELEKTRO 2.