The following data is part of a premarket notification filed by Orion Life Systems, Inc. with the FDA for Suture Removal Tray.
Device ID | K902828 |
510k Number | K902828 |
Device Name: | SUTURE REMOVAL TRAY |
Classification | Scissors, General, Surgical |
Applicant | ORION LIFE SYSTEMS, INC. 124 MESSNER DR. Wheeling, IL 60090 |
Contact | John L Laemmar |
Correspondent | John L Laemmar ORION LIFE SYSTEMS, INC. 124 MESSNER DR. Wheeling, IL 60090 |
Product Code | LRW |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-28 |
Decision Date | 1990-08-08 |