The following data is part of a premarket notification filed by Dhd Medical Products Div. Diemolding Corp. with the FDA for Nasal Cannula W/2m & 5m Tubing.
Device ID | K860872 |
510k Number | K860872 |
Device Name: | NASAL CANNULA W/2M & 5M TUBING |
Classification | Cannula, Nasal, Oxygen |
Applicant | DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. DIVISION OF DIEMOLDING CORP. Canastota, NY 13032 |
Contact | Ronald N Mchenry |
Correspondent | Ronald N Mchenry DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. DIVISION OF DIEMOLDING CORP. Canastota, NY 13032 |
Product Code | CAT |
CFR Regulation Number | 868.5340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-25 |
Decision Date | 1986-03-19 |