The following data is part of a premarket notification filed by S & W Medico Teknik with the FDA for Type 9225 Nibp.
Device ID | K890005 |
510k Number | K890005 |
Device Name: | TYPE 9225 NIBP |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | S & W MEDICO TEKNIK HERSTEDVANG 8 DK-2620 ALBERTSLUND Denmark, DK |
Contact | Lisbeth Isbrandt |
Correspondent | Lisbeth Isbrandt S & W MEDICO TEKNIK HERSTEDVANG 8 DK-2620 ALBERTSLUND Denmark, DK |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-01-03 |
Decision Date | 1989-05-11 |