The following data is part of a premarket notification filed by Cp Medical with the FDA for Dtf-1000ll,dtf-1000.
Device ID | K911118 |
510k Number | K911118 |
Device Name: | DTF-1000LL,DTF-1000 |
Classification | Syringe, Irrigating (dental) |
Applicant | CP MEDICAL P.O. BOX 5668 Huntington Beach, CA 92615 |
Contact | Carl Grodach |
Correspondent | Carl Grodach CP MEDICAL P.O. BOX 5668 Huntington Beach, CA 92615 |
Product Code | EIB |
CFR Regulation Number | 872.4565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-12 |
Decision Date | 1991-11-20 |