FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SCHNEIDER-SHILEY INFLATION SYRINGES
K Number: K861607
·
Decision Jun 9, 1986
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
56
Applicant Total
174
Review Days
41
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
- SCHNEIDER-SHILEY INFLATION SYRINGES
- K Number
- K861607
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1650
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Shiley, Inc.
- Date Received
- April 29, 1986
- Decision Date
- June 9, 1986
- Product Code
- MAV
- 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 |
|---|---|---|---|
| MAV | Syringe, Balloon Inflation | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MAV), ordered by most recent decision date.
Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)
FDA 510(k)
FDA Class 2
·Cardiovascular
Fluent inflation device
FDA 510(k)
FDA Class 2
·Cardiovascular
Everest 20 Disposable Inflation Device, Everest 20 Survival Kit, Everest 30 Disposable Inflation Device, Everest 30 Survival Kit
FDA 510(k)
FDA Class 2
·Cardiovascular
basixTOUCH40 Inflation Syringe
FDA 510(k)
FDA Class 2
·Cardiovascular
Fluent Inflation Device
FDA 510(k)
FDA Class 2
·Cardiovascular
MASTRO PLUS BALLOON IN-DEFLATION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by Shiley, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K920594 | SHILEY PERFUSION TUBING SETS | Mar 18, 1993 | Substantially Equivalent |
| K910991 | SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEM | Nov 27, 1991 | Substantially Equivalent |
| K911876 | SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200 | Aug 9, 1991 | Substantially Equivalent |
| K910923 | BCD ADVANCED | Apr 9, 1991 | Substantially Equivalent |
| K901548 | BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GAS | Jan 14, 1991 | Substantially Equivalent |
| K903435 | SHILEY SPECIALIZED TRACHEOSTOMY TUBE | Oct 2, 1990 | Substantially Equivalent |
| K901624 | SHILEY PLEXUS INTEGRAL RESERVOIR HOLLOW FIBER OXY. | Jul 3, 1990 | Substantially Equivalent |
| K901250 | PLEXUS 2(TM) INFANT HOLLOW FIBER OXYGENATOR | Jun 11, 1990 | Substantially Equivalent |
| K901249 | PLEXUS 3.5(TM) PEDIATRIC HOLLOW FIBER OXYGENATOR | Jun 11, 1990 | Substantially Equivalent |
| K900797 | STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR | May 10, 1990 | Substantially Equivalent |