The following data is part of a premarket notification filed by Dhd Medical Products Div. Diemolding Corp. with the FDA for Self-sealing Water Trap/adult/paediatric Circuits.
Device ID | K860883 |
510k Number | K860883 |
Device Name: | SELF-SEALING WATER TRAP/ADULT/PAEDIATRIC CIRCUITS |
Classification | Drain, Tee (water Trap) |
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 | BYH |
CFR Regulation Number | 868.5995 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-25 |
Decision Date | 1986-03-19 |