The following data is part of a premarket notification filed by Life-tech Intl., Inc. with the FDA for Mercury Rhinomanometer.
| Device ID | K902120 |
| 510k Number | K902120 |
| Device Name: | MERCURY RHINOMANOMETER |
| Classification | Rhinoanemometer (measurement Of Nasal Decongestion) |
| Applicant | LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
| Contact | Coats, Md |
| Correspondent | Coats, Md LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
| Product Code | BXQ |
| CFR Regulation Number | 868.1800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-05-11 |
| Decision Date | 1990-08-06 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05060485270034 | K902120 | 000 |