The following data is part of a premarket notification filed by Dhd Medical Products Div. Diemolding Corp. with the FDA for Non-rebreathing T Piece.
Device ID | K790820 |
510k Number | K790820 |
Device Name: | NON-REBREATHING T PIECE |
Classification | Valve, Non-rebreathing |
Applicant | DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CBP |
CFR Regulation Number | 868.5870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-05-01 |
Decision Date | 1979-05-04 |