The following data is part of a premarket notification filed by Air-shields, Inc. with the FDA for Satcare Oxygen Controller/monitor W/ Pulse Oximete.
Device ID | K924709 |
510k Number | K924709 |
Device Name: | SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETE |
Classification | Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia |
Applicant | AIR-SHIELDS, INC. 330 JACKSONVILLE RD. Hatboro, PA 19040 |
Contact | Francis X Casey |
Correspondent | Francis X Casey AIR-SHIELDS, INC. 330 JACKSONVILLE RD. Hatboro, PA 19040 |
Product Code | KLK |
CFR Regulation Number | 868.2500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-18 |
Decision Date | 1996-01-17 |