The following data is part of a premarket notification filed by Lsi Solutions with the FDA for Lsi Endoscopic External Accessory Channel And Accessories Product.
Device ID | K024301 |
510k Number | K024301 |
Device Name: | LSI ENDOSCOPIC EXTERNAL ACCESSORY CHANNEL AND ACCESSORIES PRODUCT |
Classification | Endoscope Channel Accessory |
Applicant | LSI SOLUTIONS 7796 VICTOR-MENDON RD. Victor, NY 14564 |
Contact | Christopher A Klaczyk |
Correspondent | Christopher A Klaczyk LSI SOLUTIONS 7796 VICTOR-MENDON RD. Victor, NY 14564 |
Product Code | ODC |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-12-24 |
Decision Date | 2003-03-24 |
Summary: | summary |