The following data is part of a premarket notification filed by Microline Pentax, Inc. with the FDA for Selecta-tip Laparoscopic Scissors.
Device ID | K970826 |
510k Number | K970826 |
Device Name: | SELECTA-TIP LAPAROSCOPIC SCISSORS |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | MICROLINE PENTAX, INC. 181 ELLIOT ST. SUITE 915 Beverly, MA 01915 |
Contact | Hughes De Laforcade |
Correspondent | Hughes De Laforcade MICROLINE PENTAX, INC. 181 ELLIOT ST. SUITE 915 Beverly, MA 01915 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-03-06 |
Decision Date | 1997-03-28 |
Summary: | summary |