The following data is part of a premarket notification filed by Artiberia with the FDA for 15-490 To 15-520 Various Splinter Forceps Peet, St.
Device ID | K851771 |
510k Number | K851771 |
Device Name: | 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST |
Classification | Forceps, General & Plastic Surgery |
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 | GEN |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-25 |
Decision Date | 1985-06-20 |