The following data is part of a premarket notification filed by Pilling Weck Group with the FDA for Reusable Trocar With Sleeve (common).
Device ID | K963815 |
510k Number | K963815 |
Device Name: | REUSABLE TROCAR WITH SLEEVE (COMMON) |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | PILLING WECK GROUP TALL PINES PARK Jaffrey, NH 03452 |
Contact | Karenann J Brozowski |
Correspondent | Karenann J Brozowski PILLING WECK GROUP TALL PINES PARK Jaffrey, NH 03452 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-23 |
Decision Date | 1996-11-05 |
Summary: | summary |