The following data is part of a premarket notification filed by Mini Lap Technologies Inc. with the FDA for Mini Lap Pediatric Instruments With Medusa Clamping System.
Device ID | K070352 |
510k Number | K070352 |
Device Name: | MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM |
Classification | Endoscopic Tissue Approximation Device |
Applicant | MINI LAP TECHNOLOGIES INC. 543 LONG HILL AVE. Shelton, CT 06484 |
Contact | Joseph Azary |
Correspondent | Joseph Azary MINI LAP TECHNOLOGIES INC. 543 LONG HILL AVE. Shelton, CT 06484 |
Product Code | OCW |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-02-06 |
Decision Date | 2007-04-05 |
Summary: | summary |