The following data is part of a premarket notification filed by Nidek Medical Products, Inc. with the FDA for Silenzio Delta Continuous Positive Airway Pressure System.
Device ID | K980551 |
510k Number | K980551 |
Device Name: | SILENZIO DELTA CONTINUOUS POSITIVE AIRWAY PRESSURE SYSTEM |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | NIDEK MEDICAL PRODUCTS, INC. 3949 VALLEY EAST INDUSTRIAL DR Birmingham, AL 35217 |
Contact | Gregg Gaskins |
Correspondent | Gregg Gaskins NIDEK MEDICAL PRODUCTS, INC. 3949 VALLEY EAST INDUSTRIAL DR Birmingham, AL 35217 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-02-12 |
Decision Date | 1998-11-17 |