The following data is part of a premarket notification filed by Equi-tron Mfg., Inc. with the FDA for Series 9000 Lift-recline Chair.
Device ID | K903905 |
510k Number | K903905 |
Device Name: | SERIES 9000 LIFT-RECLINE CHAIR |
Classification | Chair, Positioning, Electric |
Applicant | EQUI-TRON MFG., INC. 4600 WITMER INDUSTRIAL ESTATES Niagara Falls, NY 14305 |
Contact | John Porter |
Correspondent | John Porter EQUI-TRON MFG., INC. 4600 WITMER INDUSTRIAL ESTATES Niagara Falls, NY 14305 |
Product Code | INO |
CFR Regulation Number | 890.3110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-23 |
Decision Date | 1990-09-17 |