The following data is part of a premarket notification filed by Thd Spa with the FDA for Thd Disposable Anoscopes, Proctoscopes And Rectoscopes.
Device ID | K103647 |
510k Number | K103647 |
Device Name: | THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPES |
Classification | Anoscope And Accessories |
Applicant | THD SPA VIA BORGO SANTA CRISTINA 12 Imola, Bo, IT 40026 |
Contact | Guido Bonapace |
Correspondent | Guido Bonapace THD SPA VIA BORGO SANTA CRISTINA 12 Imola, Bo, IT 40026 |
Product Code | FER |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-13 |
Decision Date | 2011-03-01 |
Summary: | summary |