The following data is part of a premarket notification filed by Erich Jaeger Gmbh with the FDA for Aerosol Provocation System Aps Pro, Model Aps Pro.
| Device ID | K001502 |
| 510k Number | K001502 |
| Device Name: | AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO |
| Classification | Calculator, Pulmonary Function Data |
| Applicant | ERICH JAEGER GMBH 22705 SAVI RANCH PKWY. Yorba Linda, CA 92887 -4645 |
| Contact | Larry Murdock |
| Correspondent | Larry Murdock ERICH JAEGER GMBH 22705 SAVI RANCH PKWY. Yorba Linda, CA 92887 -4645 |
| Product Code | BZC |
| CFR Regulation Number | 868.1880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-05-15 |
| Decision Date | 2000-07-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04250892905365 | K001502 | 000 |
| 14250892903634 | K001502 | 000 |
| 04250892905372 | K001502 | 000 |
| 04250892905389 | K001502 | 000 |
| 14250892901036 | K001502 | 000 |
| 14250892902453 | K001502 | 000 |
| 14250892904525 | K001502 | 000 |
| 04250892900919 | K001502 | 000 |
| 04250892900926 | K001502 | 000 |
| 04250892900940 | K001502 | 000 |
| 04250892901022 | K001502 | 000 |
| 04250892902951 | K001502 | 000 |
| 04250892902968 | K001502 | 000 |
| 04250892902975 | K001502 | 000 |
| 04250892905341 | K001502 | 000 |
| 04250892905358 | K001502 | 000 |
| 04250892905822 | K001502 | 000 |