FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MYOCATH KIT
K Number: K780529
·
Decision May 9, 1978
Classifications
1
FEI Numbers
210
Registration Numbers
211
Same Product Code
499
Applicant Total
69
Review Days
36
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MYOCATH KIT
- K Number
- K780529
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1200
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Sorensen Research
- Date Received
- April 3, 1978
- Decision Date
- May 9, 1978
- Product Code
- DQO
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DQO | Catheter, Intravascular, Diagnostic | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DQO), ordered by most recent decision date.
Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602N
FDA 510(k)
FDA Class 2
·Cardiovascular
Arterial Pressure Monitoring Set/Tray
FDA 510(k)
FDA Class 2
·Cardiovascular
DualView Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
pNOVUS 21 Microcatheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Impress Angiographic Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by Sorensen Research
| K Number | Device Name | ||
|---|---|---|---|
| K833674 | ACCURATE MEASUREMENT DEVICE KG-AMD | Jan 25, 1984 | Substantially Equivalent |
| K833673 | ACCURATE MEASUREMENT DEVICE EZ-AMD | Dec 29, 1983 | Substantially Equivalent |
| K833095 | TRANSDUCER DOME SD105 | Nov 3, 1983 | Substantially Equivalent |
| K833094 | TRANSDUCER DOME SD104 | Nov 3, 1983 | Substantially Equivalent |
| K833096 | TRANSDUCER DOME DS106 | Nov 3, 1983 | Substantially Equivalent |
| K832957 | FLOW-DIRECTED HEPARIN COATED THERMODIL | Sep 29, 1983 | Substantially Equivalent |
| K831506 | DISP. TRANSDUCER W/MONITORING KIT TRANS | Aug 12, 1983 | Substantially Equivalent |
| K831939 | TALL FLOOR STAND TFS-01 | Jul 19, 1983 | Substantially Equivalent |
| K831505 | THORACIC GAUGE #TG-60 -VACUUM REGULATOR | Jul 12, 1983 | Substantially Equivalent |
| K820706 | WATERLESS SEAL & VACUUM REGULATOR | Apr 9, 1982 | Substantially Equivalent |