FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REGIONAL INTRAVENOUS ANESTHESIA KIT
K Number: K802290
·
Decision Oct 17, 1980
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
19
Review Days
28
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Basic Information
- Device Name
- REGIONAL INTRAVENOUS ANESTHESIA KIT
- K Number
- K802290
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5140
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Stanco Medical, Inc.
- Date Received
- September 19, 1980
- Decision Date
- October 17, 1980
- Product Code
- CAZ
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | FDA class 2 | Anesthesiology |
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Other Clearances by Stanco Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K810642 | ATRIAL-VENTRICULAR PACING ELECTRODE KIT | Apr 8, 1981 | Substantially Equivalent |
| K810643 | UNIVERSAL PACING ELECTRODE KIT | Apr 8, 1981 | Substantially Equivalent |
| K802289 | PERICARDIOCENTESIS KIT | Nov 26, 1980 | Substantially Equivalent |
| K802288 | SWAN GANZ CATHETER PLACEMENT KIT | Nov 20, 1980 | Substantially Equivalent |
| K802287 | RIGHT ATRIAL LINE KIT | Nov 20, 1980 | Substantially Equivalent |
| K802259 | TRANSVENOUS PACEMAKER ELECTRODE KIT | Oct 23, 1980 | Substantially Equivalent |
| K802326 | PRESSURE MONITORING LINES | Oct 10, 1980 | Substantially Equivalent |
| K802260 | VASCULAR CATHETER WIREGUIDES | Oct 10, 1980 | Substantially Equivalent |
| K802328 | DISP. TOUGY-BORST TYPE ADAPTOR W/PORT | Oct 10, 1980 | Substantially Equivalent |
| K802327 | SHEATH DILATOR SET | Oct 10, 1980 | Substantially Equivalent |