The following data is part of a premarket notification filed by Permobil A.b. with the FDA for Permobil Chairman L/cs 8.
Device ID | K960951 |
510k Number | K960951 |
Device Name: | PERMOBIL CHAIRMAN L/CS 8 |
Classification | Wheelchair, Powered |
Applicant | PERMOBIL A.B. BOX 120 Timra, SE S-861 23 |
Contact | Bengt Persson |
Correspondent | Bengt Persson PERMOBIL A.B. BOX 120 Timra, SE S-861 23 |
Product Code | ITI |
CFR Regulation Number | 890.3860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-03-11 |
Decision Date | 1997-04-30 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
17330818555783 | K960951 | 000 |