The following data is part of a premarket notification filed by Jedmed Instrument Co. with the FDA for Video Scope System (otoscope).
Device ID | K944031 |
510k Number | K944031 |
Device Name: | VIDEO SCOPE SYSTEM (OTOSCOPE) |
Classification | Otoscope |
Applicant | JEDMED INSTRUMENT CO. 6096 LEMAY FERRY RD. St.louis, MO 63129 -2217 |
Contact | Craig R Parks |
Correspondent | Craig R Parks JEDMED INSTRUMENT CO. 6096 LEMAY FERRY RD. St.louis, MO 63129 -2217 |
Product Code | ERA |
CFR Regulation Number | 874.4770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-17 |
Decision Date | 1994-09-23 |