Medasonics, Inc.
Mchenry, IL, US
Medasonics, Inc. appears in FDA device records in Mchenry, IL. FDA records list 19 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 19
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 19 510(k) clearances for Medasonics, Inc. between 1978 and 1999. The busiest year on record is 1980, with 3. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1979 | 1 |
| 1980 | 3 |
| 1981 | 2 |
| 1982 | 1 |
| 1983 | 3 |
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 1 |
| 1991 | 1 |
| 1992 | 1 |
| 1996 | 1 |
| 1997 | 1 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K991441 | CADENCE DOPPLER ULTRASOUND SYSTEM | KNG | Substantially Equivalent | |
| K962796 | NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEM | IYN | Substantially Equivalent | |
| K961116 | FIRST BEAT/CARDIO BEAT/CALC | IYO | Substantially Equivalent | |
| K914862 | CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDS | IYN | Substantially Equivalent | |
| K911453 | OBTRASOUND STETHOSCOPE FETAL CALC | KNG | Substantially Equivalent | |
| K882018 | MEDACORD PVL, PERSONAL VASCULAR LABORATORY | JAF | Substantially Equivalent | |
| K872292 | TRANSPECT TRANSCRANIAL DOPPLER | IYN | Substantially Equivalent | |
| K854734 | MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLE | DRM | Substantially Equivalent | |
| K833588 | VASCULAR LABORATORY TREADMILL VT1 | IOL | Substantially Equivalent | |
| K837481 | BF24 DOPPLER MODEL P872 AND P874 | Substantially Equivalent | ||
| K831393 | VASCULAB BLOOD PRESSURE CUFF | DXQ | Substantially Equivalent | |
| K820898 | VASCULAB SPECTRUM ANALYZER #SP25 | DXG | Substantially Equivalent | |
| K812609 | VASCULAB #VSC21 | JOM | Substantially Equivalent | |
| K812608 | VASCULAB #R12B | DSF | Substantially Equivalent | |
| K801549 | MODEL R11 SINGLE CHANNEL CHART RECORDER | DSF | Substantially Equivalent | |
| K800768 | VASCULAB BI-DIRECTIONAL DOPPLER, #D10 | JAF | Substantially Equivalent | |
| K800767 | MOD. MCI 17 MANUAL CUFF INFLATOR | DXQ | Substantially Equivalent | |
| K782132 | PLETHYSMOGRAPH, STRAIN GAUGE | JOM | Substantially Equivalent | |
| K781358 | SEQUENTIAL CUFF INFLATION DEVICE | JOW | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DXQBlood Pressure Cuff
- DRMCompressor, Cardiac, External
- DXGComputer, Diagnostic, Pre-Programmed, Single-Function
- KNGMonitor, Ultrasonic, Fetal
- JAFMonitor, Ultrasonic, Nonfetal
- JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic
- DSFRecorder, Paper Chart
- JOWSleeve, Limb, Compressible
- IYNSystem, Imaging, Pulsed Doppler, Ultrasonic
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- IOLTreadmill, Powered
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
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Is this your company?
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Data as of , FDA export datePage updated Source: openFDA, public domain
