The following data is part of a premarket notification filed by Microline Pentax, Inc. with the FDA for 3 Mm Selec-tip Laparoscopic Scissors.
Device ID | K980758 |
510k Number | K980758 |
Device Name: | 3 MM SELEC-TIP LAPAROSCOPIC SCISSORS |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | MICROLINE PENTAX, INC. 70 WALNUT ST. Wellesley, MA 02481 -2102 |
Contact | Jacqueline E Masse |
Correspondent | Jacqueline E Masse MICROLINE PENTAX, INC. 70 WALNUT ST. Wellesley, MA 02481 -2102 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-02-27 |
Decision Date | 1998-03-27 |
Summary: | summary |