K & S Medicorp
Country not established
- Devices
- 3
What K & S Medicorp makes
K & S Medicorp manufactures medical devices for auscultation, including the SALTZMAN EAR™ endotracheal auscultation receptor, the TRANSCOR™ radio-stethoscope, and the SALTZMAN stethoscope head. These products are designed for clinical assessment of lung and heart sounds, with applications in critical care and patient monitoring.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
Transcor (Tm) Radio-Stethoscope Ref K854772
510(k) 510(k)Saltzman Stethoscope Head Ref K854771
510(k) 510(k)
Frequently asked questions
How many devices does K & S Medicorp have in the registry?
The registry currently lists 3 devices for K & S Medicorp. Devices recorded under merged duplicate company entries are counted once.
Which registries list K & S Medicorp's devices?
Among its 3 most recently registered devices, K & S Medicorp has devices listed in FDA 510(k) (3 devices).
What risk classes do K & S Medicorp's devices fall under?
Among its 3 most recently registered devices, the classes recorded for K & S Medicorp's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from K & S Medicorp in the registry?
The most recently registered devices listed for K & S Medicorp include SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR, TRANSCOR (TM) RADIO-STETHOSCOPE and SALTZMAN STETHOSCOPE HEAD.