The following data is part of a premarket notification filed by Applied Medical Technologies with the FDA for Gastrointestinal Tubes & Accessories.
Device ID | K945618 |
510k Number | K945618 |
Device Name: | GASTROINTESTINAL TUBES & ACCESSORIES |
Classification | Tubes, Gastrointestinal (and Accessories) |
Applicant | APPLIED MEDICAL TECHNOLOGIES 6100 WEST CREEK RD. SUITE 25 Independence, OH 44131 |
Contact | Donna Bressan |
Correspondent | Donna Bressan APPLIED MEDICAL TECHNOLOGIES 6100 WEST CREEK RD. SUITE 25 Independence, OH 44131 |
Product Code | KNT |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-15 |
Decision Date | 1995-10-12 |