KOKOMATE
Spirometer, Diagnostic
FERRARIS RESPIRATORY, INC.
The following data is part of a premarket notification filed by Ferraris Respiratory, Inc. with the FDA for Kokomate.
Pre-market Notification Details
| Device ID | K022276 |
| 510k Number | K022276 |
| Device Name: | KOKOMATE |
| Classification | Spirometer, Diagnostic |
| Applicant | FERRARIS RESPIRATORY, INC. 908 MAIN ST. Louisville, CO 80027 |
| Contact | Jim Lewis |
| Correspondent | Jim Lewis FERRARIS RESPIRATORY, INC. 908 MAIN ST. Louisville, CO 80027 |
| Product Code | BZG |
| CFR Regulation Number | 868.1840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-15 |
| Decision Date | 2002-10-04 |
| Summary: | summary |
Trademark Results [KOKOMATE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KOKOMATE 73196329 1161191 Dead/Cancelled |
Moxie Industries, Inc. 1978-12-07 |
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