Texas Medical Products, Inc.
Mchenry, IL, US
Texas Medical Products, Inc. appears in FDA device records in Mchenry, IL. FDA records list 30 510(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
- 30
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 30 510(k) clearances for Texas Medical Products, Inc. between 1980 and 1989. The busiest year on record is 1980, with 16. The most recent is 1989, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 16 |
| 1981 | 9 |
| 1982 | 1 |
| 1983 | 1 |
| 1985 | 1 |
| 1987 | 1 |
| 1989 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K893417 | SURGIFRESH SUB-MICRON MASK NO. 901008-000 | FXX | Substantially Equivalent | |
| K870932 | SURGIFRESH SURGICAL SMOKE REMOVAL | Substantially Equivalent | ||
| K851575 | DR. BRUNO LNAGE MINI PHOTOMETER | Substantially Equivalent | ||
| K830634 | CARDIOTOMY FILTER | JOD | Substantially Equivalent | |
| K813587 | DISPOSABLE THORACIC CATHETER | GBS | Substantially Equivalent | |
| K810532 | DISPOSABLE STOPCOCK | DTZ | Substantially Equivalent | |
| K810515 | DISPOSABLE 2-STAGE CANNULA | DWF | Substantially Equivalent | |
| K810395 | PRE-BYPASS FILTER | KRJ | Substantially Equivalent | |
| K802545 | CARDIOPLEGIC SETS | DTR | Substantially Equivalent | |
| K802544 | DISPOSABLE QUICK RELEASE PERFUSION ADAP | DTL | Substantially Equivalent | |
| K802543 | RIDGID VENA CAVA CANNULAE | DWF | Substantially Equivalent | |
| K802542 | DISPOSABLE CONNECTORS | KRI | Substantially Equivalent | |
| K802541 | DISPOSABLE PARALLEL Y CONNECTORS | KRI | Substantially Equivalent | |
| K802539 | DISPOSABLE GAS LINE FILTER | KRI | Substantially Equivalent | |
| K802537 | DISPOSABLE SURGICAL DRAPE | KKX | Substantially Equivalent | |
| K802538 | BASIN PACK | FNY | Substantially Equivalent | |
| K801405 | DISPOSABLE PERFUSION CONNECTORS | DTL | Substantially Equivalent | |
| K801404 | DISPOSABLE PARALLEL Y CONNECTORS | DTL | Substantially Equivalent | |
| K801403 | DISPOSABLE PERFUSION SET | DWF | Substantially Equivalent | |
| K801402 | QUICKIE PRIME CARDIOP. BYPASS PERF. INTR | DTL | Substantially Equivalent | |
| K801401 | CARDIOPULMONARY BYPASS TUBING | DWF | Substantially Equivalent | |
| K801400 | DISPOSABLE SUCKER SYSTEM | DTS | Substantially Equivalent | |
| K801399 | CORONARY PERFUSION CONNECTOR PLUG | DTL | Substantially Equivalent | |
| K801398 | AORTIC AND FEMORAL PERFUSION CANNULAE | DWF | Substantially Equivalent | |
| K801397 | VENA CAVA CANNULAE | DWF | Substantially Equivalent | |
| K801396 | SAPHENOUS VEIN CANNULAE | DWF | Substantially Equivalent | |
| K801395 | VASCULAR CLAMP | DXC | Substantially Equivalent | |
| K801394 | CARDIOPULMONARY BYPASS PUMP TUBING | DWE | Substantially Equivalent | |
| K801393 | AIR ASPIRATOR NEEDLE | DWS | Substantially Equivalent | |
| K801392 | DISPOSABLE SUMP SETS | DWF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KRIAccessory Equipment, Cardiopulmonary Bypass
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- FNYBasin, Emesis
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- GBSCatheter, Ventricular, General & Plastic Surgery
- DXCClamp, Vascular
- KKXDrape, Surgical, Antimicrobial
- JODFilter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
- KRJFilter, Prebypass, Cardiopulmonary Bypass
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- DWSInstruments, Surgical, Cardiovascular
- FXXMask, Surgical
- DTZOxygenator, Cardiopulmonary Bypass
- DTSSucker, Cardiotomy Return, Cardiopulmonary Bypass
- DWETubing, Pump, Cardiopulmonary Bypass
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain
