FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SCIMED PM200 INFLATION MANOMETER
K Number: K843448
·
Decision Oct 23, 1984
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
56
Applicant Total
109
Review Days
48
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
- SCIMED PM200 INFLATION MANOMETER
- K Number
- K843448
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1650
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Scimed Life Systems, Inc.
- Date Received
- September 5, 1984
- Decision Date
- October 23, 1984
- 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 Scimed Life Systems, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K974241 | SCIMED INFORMER PRESSURE WIRE SYSTEM | Nov 12, 1998 | Substantially Equivalent |
| K981788 | SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETER | Aug 18, 1998 | Substantially Equivalent |
| K980360 | SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRES | Apr 29, 1998 | Substantially Equivalent |
| K974559 | SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS | Feb 23, 1998 | Substantially Equivalent |
| K974684 | SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER | Feb 19, 1998 | Substantially Equivalent |
| K973945 | LUGE GUIDE WIRE | Jan 12, 1998 | Substantially Equivalent |
| K970823 | SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER | Jun 3, 1997 | Substantially Equivalent |
| K964551 | CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID | May 21, 1997 | Substantially Equivalent |
| K970244 | SCIMED CHOICE FAMILY OF PTCA GUIDE WIRES | Mar 28, 1997 | Substantially Equivalent |
| K965023 | CHOICE PT PLUS PTCA GUIDE WIRE AND CHOICE PT VISION PTCA GUIDE WIRE | Mar 4, 1997 | Substantially Equivalent |