Life-Tech Instruments, Inc.
Mchenry, IL, US
Life-Tech Instruments, 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 Life-Tech Instruments, Inc. between 1977 and 1981. The busiest year on record is 1978, with 9. The most recent is 1981, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 3 |
| 1978 | 9 |
| 1979 | 2 |
| 1980 | 1 |
| 1981 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K812177 | LIFE-TECH #1857 PRESSURE/POLOT MODULE | EXQ | Substantially Equivalent | |
| K812179 | LIFE-TECH #1753 BIOFEEDBACK TRAINER | HCC | Substantially Equivalent | |
| K812180 | LIFE-TECH #5102 VISULAB | GWN | Substantially Equivalent | |
| K812178 | LIFE-TECH #'S 1106/1156 UROLABS | FAP | Substantially Equivalent | |
| K800112 | AMBLYOPIA TRAINER | HPL | Substantially Equivalent | |
| K790663 | MODEL 1750 STANDING URINAL | FFG | Substantially Equivalent | |
| K790664 | MODEL 1309 AUDIO MONITOR | IKN | Substantially Equivalent | |
| K781476 | MULAR GOLD LEAF ELECTRODE MODEL 7501 | HLZ | Substantially Equivalent | |
| K781461 | MODEL 7320 VISUAL STIMULATOR | GWE | Substantially Equivalent | |
| K781475 | ELECTRODE IMPEDANCE TESTER-MODEL 500 | GYA | Substantially Equivalent | |
| K781474 | PREAMPLIFIER MODELS 8101PI & 8102PI | EWO | Substantially Equivalent | |
| K780539 | STIMULATOR MODEL 8021 | GWF | Substantially Equivalent | |
| K780537 | EAR ELECTRODE-ADULT & PEDIATRIC | GXY | Substantially Equivalent | |
| K780541 | PRESSURE MODULES MODELS 1855 & 1856 | IKN | Substantially Equivalent | |
| K780540 | ELECTRIC RESPONSE AUDIOMETER | GWJ | Substantially Equivalent | |
| K780538 | AUDIO MONITOR-MODEL 8309 | GWK | Substantially Equivalent | |
| K770897 | URODYNAMIC INSTRUMENTS | EXY | Substantially Equivalent | |
| K770579 | CATHETER, URETHRAL PRESSURE, UPE-10 & 12 | FAP | Substantially Equivalent | |
| K770268 | SYS. FOR REC. BSER RESPONSES | GWJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EWOAudiometer
- GWKConditioner, Signal, Physiological
- EXQCystometer, Electrical Recording
- FAPCystometric Gas (Carbon-Dioxide) On Hydraulic Device
- HCCDevice, Biofeedback
- HPLDevice, Fixation, Ac-Powered, Ophthalmic
- FFGDevice, Urine Flow Rate Measuring, Non-Electrical, Disposable
- HLZElectrode, Corneal
- GXYElectrode, Cutaneous
- IKNElectromyograph, Diagnostic
- GWNNystagmograph
- GWJStimulator, Auditory, Evoked Response
- GWFStimulator, Electrical, Evoked Response
- GWEStimulator, Photic, Evoked Response
- GYATester, Electrode/Lead, Electroencephalograph
- EXYUroflowmeter
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain