The following data is part of a premarket notification filed by Artiberia with the FDA for 1070/15 To 1078/17 Various Types Needle Holders.
Device ID | K851719 |
510k Number | K851719 |
Device Name: | 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS |
Classification | Prosthesis, Vas Deferens |
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 | EZZ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-25 |
Decision Date | 1985-07-02 |