The following data is part of a premarket notification filed by Artiberia with the FDA for 25-100,25-220 Various Needle Holders.
Device ID | K851779 |
510k Number | K851779 |
Device Name: | 25-100,25-220 VARIOUS NEEDLE HOLDERS |
Classification | Holder, Needle, Gastroenterologic |
Applicant | ARTIBERIA 4518 LOS RANCHITOS San Antonio, TX 78233 |
Contact | Gil M Sanchez |
Correspondent | Gil M Sanchez ARTIBERIA 4518 LOS RANCHITOS San Antonio, TX 78233 |
Product Code | FHQ |
CFR Regulation Number | 876.4730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-25 |
Decision Date | 1985-06-20 |