The following data is part of a premarket notification filed by Future Impex Corp. with the FDA for Pm-80 Pulmotester.
Device ID | K843984 |
510k Number | K843984 |
Device Name: | PM-80 PULMOTESTER |
Classification | Spirometer, Diagnostic |
Applicant | FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deerpark, NY 11729 |
Contact | Morad Davoudzadeh |
Correspondent | Morad Davoudzadeh FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deerpark, NY 11729 |
Product Code | BZG |
CFR Regulation Number | 868.1840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-10-11 |
Decision Date | 1984-10-24 |