The following data is part of a premarket notification filed by Research Medical, Inc. with the FDA for Rmi Surgiccal Site Visualization Wand.
Device ID | K922083 |
510k Number | K922083 |
Device Name: | RMI SURGICCAL SITE VISUALIZATION WAND |
Classification | Lavage, Jet |
Applicant | RESEARCH MEDICAL, INC. 6864 SOUTH 300 WEST Midvale, UT 84047 |
Contact | Rd Hibbert |
Correspondent | Rd Hibbert RESEARCH MEDICAL, INC. 6864 SOUTH 300 WEST Midvale, UT 84047 |
Product Code | FQH |
CFR Regulation Number | 880.5475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-04 |
Decision Date | 1993-01-29 |