The following data is part of a premarket notification filed by Reliance Medical Products, Inc. with the FDA for Reliance(r) 6200 Examination Chair.
Device ID | K894018 |
510k Number | K894018 |
Device Name: | RELIANCE(R) 6200 EXAMINATION CHAIR |
Classification | Chair, Ophthalmic, Ac-powered |
Applicant | RELIANCE MEDICAL PRODUCTS, INC. 96 CALDWELL DR. CINCINNATI, OH 45216 |
Contact | RICHARD G TAYLOR |
Correspondent | RICHARD G TAYLOR RELIANCE MEDICAL PRODUCTS, INC. 96 CALDWELL DR. CINCINNATI, OH 45216 |
Product Code | HME |
CFR Regulation Number | 886.1140 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-06-06 |
Decision Date | 1989-09-12 |