The following data is part of a premarket notification filed by Rifton with the FDA for Mechanical Tables And Accessories.
Device ID | K882900 |
510k Number | K882900 |
Device Name: | MECHANICAL TABLES AND ACCESSORIES |
Classification | Table, Mechanical |
Applicant | RIFTON ROUTE 213 Rifton, NY 12471 |
Contact | John Rhodes |
Correspondent | John Rhodes RIFTON ROUTE 213 Rifton, NY 12471 |
Product Code | INW |
CFR Regulation Number | 890.3750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-07-11 |
Decision Date | 1988-08-19 |