The following data is part of a premarket notification filed by Richard Wolf Medical Instruments Corp. with the FDA for Flexible Video Cystoscope/choledochoscope, Models 7308.061 And 7308.066.
Device ID | K051176 |
510k Number | K051176 |
Device Name: | FLEXIBLE VIDEO CYSTOSCOPE/CHOLEDOCHOSCOPE, MODELS 7308.061 AND 7308.066 |
Classification | Cystoscope And Accessories, Flexible/rigid |
Applicant | RICHARD WOLF MEDICAL INSTRUMENTS CORP. 353 CORPORATE WOODS PKWY. Vernon Hills, IL 60061 |
Contact | Robert L Casarsa |
Correspondent | Robert L Casarsa RICHARD WOLF MEDICAL INSTRUMENTS CORP. 353 CORPORATE WOODS PKWY. Vernon Hills, IL 60061 |
Product Code | FAJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-06 |
Decision Date | 2005-10-05 |
Summary: | summary |