Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- DQFActuator, Syringe, Injector Type2Product Code
- DQIWithdrawal/Infusion Pump2Product Code
- K960486KSEA MODEL 383320 20 ANGIOMAT2Cleared 510(K)
- K935763SURGIPUMP2Cleared 510(K)
- K922541USCI SUPER 9 PTCA GUIDING CATHETER2Cleared 510(K)
- K924110LEOCOR CORFLO PUMP -- MODIFICATION2Cleared 510(K)
- K905189BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)2Cleared 510(K)
- K902444CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP2Cleared 510(K)
- K895688NOBLES-LAI ENGINEERING INFUSION PUMP2Cleared 510(K)
- K895074ANGIOSCOPY PUMP2Cleared 510(K)
- K871422OLYMPUS ANGIOSCOPY PUMP2Cleared 510(K)
- DXTInjector And Syringe, Angiographic2Product Code
- IZQInjector, Contrast Medium, Automatic2Product Code
- NKPInjector, Contrast Medium, Automatic, Reprocessed2Product Code
- NKTInjector And Syringe, Angiographic, Reprocessed2Product Code
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart C—General Hospital and Personal Use Monitoring DevicesCFR Sub-Part
- Subpart D—Pathology Instrumentation and AccessoriesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- HematologyReview Panel
- ImmunologyReview Panel
- MicrobiologyReview Panel
- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
LEOCOR CORFLO PUMP -- MODIFICATION
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K924110
- 510(k) Type
- Traditional
- Applicant
- LEOCOR, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 9/1/1992
- Days to Decision
- 90 days
- Submission Type
- Statement