Data / Medical devices / United States / Life Sensing Instruments, Inc.
Life Sensing Instruments, Inc.: FDA-registered device maker in Charlotte, NC, United States, 1 510(k) clearance
Life Sensing Instruments, Inc. is registered with the FDA (registration 1037137) in Charlotte, NC, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 19, 1990. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1037137
- Address
- 2102 Cambridge Beltway Dr Ste A1, Charlotte, NC, United States, 28273
- Owner or operator
- LIFE SENSING INSTRUMENTS, INC. (1037137)
- Roles
- Manufacturer
- First device listed
- December 11, 2007
- Registered through
- 2026
- Brand names listed
- HTS 820
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Detector And Alarm, Arrhythmia | DSI | 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 |
|---|---|---|---|---|---|---|
| March 19, 1990 | K896967 | HTS 820 CARDIAC MONITOR | DSI | Substantially Equivalent | Life Sensing Instrument Company, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 19, 1990. 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.