The following data is part of a premarket notification filed by Roseburg Sa with the FDA for Portaspir Ii.
Device ID | K851560 |
510k Number | K851560 |
Device Name: | PORTASPIR II |
Classification | Pump, Portable, Aspiration (manual Or Powered) |
Applicant | ROSEBURG SA 1054 31ST STREET, N.W. SUITE 120 CANAL SQUARE Washington, DC 20007 |
Contact | Chambord |
Correspondent | Chambord ROSEBURG SA 1054 31ST STREET, N.W. SUITE 120 CANAL SQUARE Washington, DC 20007 |
Product Code | BTA |
CFR Regulation Number | 878.4780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-16 |
Decision Date | 1985-12-13 |