The following data is part of a premarket notification filed by Percussionaire Corp. with the FDA for Percussionaire(r) Oscillatron-1 Percuss 1300 Min.
Device ID | K900314 |
510k Number | K900314 |
Device Name: | PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN |
Classification | Ventilator, Continuous, Facility Use |
Applicant | PERCUSSIONAIRE CORP. BIRD AIRLODGE, GLENGARY BAY P.O. BOX 817 Sandpoint, ID 83864 |
Contact | Bird, Md |
Correspondent | Bird, Md PERCUSSIONAIRE CORP. BIRD AIRLODGE, GLENGARY BAY P.O. BOX 817 Sandpoint, ID 83864 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-22 |
Decision Date | 1990-10-26 |