The following data is part of a premarket notification filed by Permobil Ab with the FDA for F5 Corpus Vs.
Device ID | K191874 |
510k Number | K191874 |
Device Name: | F5 Corpus VS |
Classification | Wheelchair, Standup |
Applicant | Permobil AB Box 120 S-861 23 Timra, SE |
Contact | Ivan Fernandez |
Correspondent | Ivan Fernandez Permobil AB Box 120 S-861 23 Timra, SE |
Product Code | IPL |
CFR Regulation Number | 890.3900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-07-12 |
Decision Date | 2019-10-25 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
17330818001006 | K191874 | 000 |
17330818002003 | K191874 | 000 |