The following data is part of a premarket notification filed by Williams Manufacturing Co. with the FDA for Zenith Traveler Chiropractic Table.
Device ID | K880222 |
510k Number | K880222 |
Device Name: | ZENITH TRAVELER CHIROPRACTIC TABLE |
Classification | Table, Mechanical |
Applicant | WILLIAMS MANUFACTURING CO. 158 N. EDISON AVE. Elgin, IL 60123 |
Contact | Wayne L Peterson |
Correspondent | Wayne L Peterson WILLIAMS MANUFACTURING CO. 158 N. EDISON AVE. Elgin, IL 60123 |
Product Code | INW |
CFR Regulation Number | 890.3750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-01-20 |
Decision Date | 1988-02-03 |