Erich Jaeger, Inc.
Yorba Linda, CA, US
Erich Jaeger, Inc. appears in FDA device records in Yorba Linda, CA. FDA records list 36 510(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
- 36
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 36 510(k) clearances for Erich Jaeger, Inc. between 1984 and 2003. The busiest year on record is 1984, with 15. The most recent is 2003, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 15 |
| 1985 | 4 |
| 1986 | 4 |
| 1994 | 2 |
| 1996 | 1 |
| 1998 | 2 |
| 1999 | 1 |
| 2000 | 4 |
| 2003 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023120 | OXYCON MOBILE | BZC | Substantially Equivalent | |
| K023796 | MS PAED-BABY BODY | CCM | Substantially Equivalent | |
| K021138 | SLEEPSCREEN/APNOESCREEN CARDIO | MNR | Substantially Equivalent | |
| K000396 | APNOESCREEN PRO, ALPHA SCREEN PRO | MNR | Substantially Equivalent | |
| K001502 | AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO | BZC | Substantially Equivalent | |
| K000648 | SPIRO PRO | BTY | Substantially Equivalent | |
| K992214 | OXYCON PRO | BZC | Substantially Equivalent | |
| K984465 | OXYCONALPHA WITH OPTION ECG | LOS | Substantially Equivalent | |
| K980094 | MODIFICATION TO THE OXYCONALPHA | BTY | Substantially Equivalent | |
| K972419 | TOENNIES NEUROSCREEN SYSTEM | IKN | Substantially Equivalent | |
| K960078 | ASTHMA MONITOR | BZG | Substantially Equivalent | |
| K933839 | MASTER SCREEN PNUEMO | BTY | Substantially Equivalent | |
| K932744 | FLOWSCREEN | BTY | Substantially Equivalent | |
| K853443 | ALVEO-DIFFUSION TEST | BZC | Substantially Equivalent | |
| K853434 | ERGO-PNEUMOTEST | BZL | Substantially Equivalent | |
| K853409 | SCREENMATE | BZG | Substantially Equivalent | |
| K853390 | INFANT BODY TEST | CCM | Substantially Equivalent | |
| K853360 | N20 TEST | CBR | Substantially Equivalent | |
| K852337 | PNEUMOSCOPE | BZG | Substantially Equivalent | |
| K843851 | BODYSCREEN II | CCM | Substantially Equivalent | |
| K843846 | UNIVERSAL-BODYTEST | CCM | Substantially Equivalent | |
| K843860 | OXYSCREEN | BZC | Substantially Equivalent | |
| K843841 | ERGO-OXYSCREEN | BZG | Substantially Equivalent | |
| K843843 | HE TEST | BSE | Substantially Equivalent | |
| K843859 | LAUF-ERGOTEST JUNIOR | IOL | Substantially Equivalent | |
| K843855 | ERGOTEST 40 & 45 | ISP | Substantially Equivalent | |
| K843853 | LAUF-ERGOTEST | IOL | Substantially Equivalent | |
| K843850 | UNIVERSAL-ERGOTEST | ISD | Substantially Equivalent | |
| K843857 | TRANSFERSCREEN II | Substantially Equivalent | ||
| K843852 | APTA-BRONCHOSCREEN | BZC | Substantially Equivalent | |
| K843848 | AW TEST | BZC | Substantially Equivalent | |
| K843849 | PNEUMOSCREEN | BZC | Substantially Equivalent | |
| K843847 | O2 TEST | CCL | Substantially Equivalent | |
| K843845 | CO TEST | CCJ | Substantially Equivalent | |
| K843844 | CO2 TEST | CCK | Substantially Equivalent | |
| K843840 | N2 TEST | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- CCJAnalyzer, Gas, Carbon-Monoxide, Gaseous-Phase
- BSEAnalyzer, Gas, Helium, Gaseous-Phase
- CBRAnalyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.)
- CCLAnalyzer, Gas, Oxygen, Gaseous-Phase
- BTYCalculator, Predicted Values, Pulmonary Function
- BZCCalculator, Pulmonary Function Data
- BZLComputer, Oxygen-Uptake
- IKNElectromyograph, Diagnostic
- ISDExerciser, Measuring
- CCMPlethysmograph, Pressure
- BZGSpirometer, Diagnostic
- IOLTreadmill, Powered
- ISPValve, Prosthesis
- MNRVentilatory Effort Recorder
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