Hospitak, Inc.
Mchenry, IL, US
Hospitak, Inc. appears in FDA device records in Mchenry, IL. FDA records list 27 510(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
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Hospitak, Inc. between 1978 and 1996. The busiest year on record is 1979, with 5. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 3 |
| 1979 | 5 |
| 1980 | 3 |
| 1983 | 2 |
| 1984 | 5 |
| 1985 | 1 |
| 1987 | 1 |
| 1992 | 2 |
| 1994 | 1 |
| 1995 | 2 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K955483 | TRACH MASK MODEL (245, 246) | BYF | Substantially Equivalent | |
| K954787 | ILLUMINATOR | CCW | Substantially Equivalent | |
| K953620 | WARM N WET HMEF W/LUER ADAPTER | BYD | Substantially Equivalent | |
| K953619 | WARM N WET HME W/LUER ADAPTER | BYD | Substantially Equivalent | |
| K915750 | DISPOSABLE BACTERIAL BREATHNG FILTER | CAH | Substantially Equivalent | |
| K920842 | AEROSOL DELIVERY SYSTEMS | LRD | Substantially Equivalent | |
| K915228 | DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL | CCK | Substantially Equivalent | |
| K873286 | DISPOSABLE, MANUAL PULMONARY RESUSCITATOR | BTM | Substantially Equivalent | |
| K853600 | INFLATABLE AIR SPLINTS | FZF | Substantially Equivalent | |
| K844328 | OXYGEN CONCENTRATOR | CAW | Substantially Equivalent | |
| K843212 | LOW PRESSURE ALARM FOR OXYGEN CYLINDER | BXH | Substantially Equivalent | |
| K840817 | DISPOSABLE, HYPERBARIC OXYGEN CHAMBER | KPJ | Substantially Equivalent | |
| K840276 | DISPOSABLE, PRESSURE RELIEF VALVE | Substantially Equivalent | ||
| K841240 | DISPOSABLE ANESTHESIA MASK | BSJ | Substantially Equivalent | |
| K831825 | DISPOS. HYPERBARIC OXYGEN CUSH/TRAUM | KPJ | Substantially Equivalent | |
| K831270 | DISPOS. MEDICATION NEBULIZER | CAF | Substantially Equivalent | |
| K802062 | SOF-TOUCH NASAL CANNULA CAT.#304 & 305 | CAT | Substantially Equivalent | |
| K792426 | DISPOSABLE TEMPERATURE PROBE | FLK | Substantially Equivalent | |
| K792598 | DISPOSABLE INCENTIVE SPIROMETER | BWF | Substantially Equivalent | |
| K791539 | DISPOSABLE 22MM ADAPTOR | BZA | Substantially Equivalent | |
| K791538 | DISPOSABLE AEROSOL T | BZA | Substantially Equivalent | |
| K791537 | DISPOSABLE MOUTHPIECE | BYP | Substantially Equivalent | |
| K791536 | DISPOSABLE MEDICATION NEBULIZER | CAF | Substantially Equivalent | |
| K791469 | MANIFOLD/NEBULIZER BREATHING PRODUCTS | BZO | Substantially Equivalent | |
| K781908 | BREATHING CIRCUIT PRODUCTS, ANESTHESIA | CAI | Substantially Equivalent | |
| K781055 | FACE TENTS | BYG | Substantially Equivalent | |
| K780626 | VENTURI OXYGEN MASK | BYF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- LRDApplicator, Ent Drug
- CATCannula, Nasal, Oxygen
- KPJChamber, Oxygen, Topical, Extremity
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- BYDCondenser, Heat And Moisture (Artificial Nose)
- BZAConnector, Airway (Extension)
- CAHFilter, Bacterial, Breathing-Circuit
- BXHGauge, Gas Pressure, Cylinder/Pipeline
- CAWGenerator, Oxygen, Portable
- CCWLaryngoscope, Rigid
- BSJMask, Gas, Anesthetic
- BYGMask, Oxygen
- BYFMask, Oxygen, Low Concentration, Venturi
- BYPMouthpiece, Breathing
- CAFNebulizer (Direct Patient Interface)
- BZOSet, Tubing And Support, Ventilator (W Harness)
- BWFSpirometer, Therapeutic (Incentive)
- FZFSplint, Extremity, Inflatable, External
- FLKThermometer, Clinical Mercury
- BTMVentilator, Emergency, Manual (Resuscitator)
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