The following data is part of a premarket notification filed by Hill Laboratories Co. with the FDA for The Hill Hi-lo Table.
Device ID | K934754 |
510k Number | K934754 |
Device Name: | THE HILL HI-LO TABLE |
Classification | Table, Powered |
Applicant | HILL LABORATORIES CO. 445 LINCOLN HIGHWAY Malvern, PA 19355 |
Contact | Howard A Hill |
Correspondent | Howard A Hill HILL LABORATORIES CO. 445 LINCOLN HIGHWAY Malvern, PA 19355 |
Product Code | INQ |
CFR Regulation Number | 890.3760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-04 |
Decision Date | 1995-02-17 |