Leocor, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Leocor, Inc. makes
Leocor, Inc. manufactures guiding catheters and infusion pumps designed for interventional cardiology procedures. Their products include a guiding catheter for vascular access and a range of CORFLO pumps and catheters, which are used in percutaneous transluminal coronary angioplasty (PTCA) and related interventions.
The company’s devices are classified as Class II under FDA regulations and are authorised through 510(k) clearances and Premarket Approval Applications (PMA). These products are listed in the FDA’s regulatory databases, and the company is headquartered in the United States.
Catalogue
Leocor Guiding Catheter Ref K911270
Regimes: 510(k) Registry: 510(k)Leocor Corflo Pump -- Modification Ref K924110
Regimes: 510(k) Registry: 510(k)Leocor Corflo(Tm) Pump Ref K900350
Regimes: 510(k) Registry: 510(k)Leocor Corflo(Tm) Model 7.5PT Ptca Catheter Ref P890001
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Leocor, Inc. have in the registry?
The registry currently lists 4 devices for Leocor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leocor, Inc.'s devices?
Among its 4 most recently registered devices, Leocor, Inc. has devices listed in FDA 510(k) (3 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Leocor, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Leocor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leocor, Inc. in the registry?
The most recently registered devices listed for Leocor, Inc. include LEOCOR GUIDING CATHETER, LEOCOR CORFLO PUMP -- MODIFICATION, LEOCOR CORFLO(TM) PUMP and LEOCOR CORFLO(TM) MODEL 7.5PT PTCA CATHETER.