FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STOPCOCK, ONE WAY
K Number: K770383
·
Decision Mar 7, 1977
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
181
Applicant Total
77
Review Days
7
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
- STOPCOCK, ONE WAY
- K Number
- K770383
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5820
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Cobe Laboratories, Inc.
- Date Received
- February 28, 1977
- Decision Date
- March 7, 1977
- Product Code
- KOC
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| KOC | Accessories, Blood Circuit, Hemodialysis | FDA class 2 | Gastroenterology, Urology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KOC), ordered by most recent decision date.
BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series (AL-ADC-E(U), AL-CDC-E(U), C18RDC-E(U), C18BDD-E(U), C18SFD-E(U)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series AL-ADC-PU, AL-CDC-PU, C18RDC-PU, C18BDD-PU, C18SFD-PU
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Blood Tubing Lines for Hemodialysis AV06C-E
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Blood Tubing Lines for Hemodialysis AL Series (Archloop), Blood Tubing Lines for Hemodialysis C18 Series
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Integrated Crit-Line Technology, CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Intergrated Crit-Line Technology, no Heparin Line
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CAREline Airless Hemodialysis Blood Tubing Sets
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Other Clearances by Cobe Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K923272 | COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATOR | May 11, 1993 | Substantially Equivalent |
| K900105 | COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC | Mar 22, 1991 | Substantially Equivalent |
| K905793 | COBE CENTRY 2 BICART OPTION KIT | Feb 12, 1991 | Substantially Equivalent |
| K905388 | COBE CENTRYSYSTEM 3 BICART OPTION KIT | Feb 11, 1991 | Substantially Equivalent |
| K904336 | NEW COBE SATURATION/HEMATOCRIT MONITOR | Dec 27, 1990 | Substantially Equivalent |
| K902631 | COBE ICU CONVERSION KIT | Dec 17, 1990 | Substantially Equivalent |
| K902437 | COBE CARDIOTOMY RESERVOIR WITH OR WITHOUT FILTER | Dec 17, 1990 | Substantially Equivalent |
| K904566 | NEW COBE CENTRYSYSTEM(TM) 100 HG DIALYZER | Dec 12, 1990 | Substantially Equivalent |
| K902758 | COBE SATURATION/HEMATOCRIT MONITOR W/ FIBER OPTIC | Aug 23, 1990 | Substantially Equivalent |
| K902759 | COBE CLOSED WOUND DRAINAGE KIT | Jul 18, 1990 | Substantially Equivalent |