The following data is part of a premarket notification filed by Altimate Medical, Inc. with the FDA for Easystand Bantam Medium.
Device ID | K123834 |
510k Number | K123834 |
Device Name: | EASYSTAND BANTAM MEDIUM |
Classification | Chair, Positioning, Electric |
Applicant | ALTIMATE MEDICAL, INC. 262 WEST FIRST ST. Morton, MN 56270 |
Contact | Stacey Frank |
Correspondent | Stacey Frank ALTIMATE MEDICAL, INC. 262 WEST FIRST ST. Morton, MN 56270 |
Product Code | INO |
CFR Regulation Number | 890.3110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-12-13 |
Decision Date | 2013-08-13 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10858921006055 | K123834 | 000 |