The following data is part of a premarket notification filed by Surgiquest, Inc. with the FDA for Surgiquest Airseal Optical Trocar And Cannula System.
Device ID | K092504 |
510k Number | K092504 |
Device Name: | SURGIQUEST AIRSEAL OPTICAL TROCAR AND CANNULA SYSTEM |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | SURGIQUEST, INC. 12 CASCADE BLVD. SUITE 2B Orange, CT 06477 |
Contact | Kourosh Azarbarzin |
Correspondent | Kourosh Azarbarzin SURGIQUEST, INC. 12 CASCADE BLVD. SUITE 2B Orange, CT 06477 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-08-14 |
Decision Date | 2009-11-05 |