The following data is part of a premarket notification filed by U.s. Dentek Corp. with the FDA for Dental Pik.
Device ID | K892861 |
510k Number | K892861 |
Device Name: | DENTAL PIK |
Classification | File, Pulp Canal, Endodontic |
Applicant | U.S. DENTEK CORP. 32 LEVERONI CT. #101 Novato, CA 94949 |
Contact | John M Jansheski |
Correspondent | John M Jansheski U.S. DENTEK CORP. 32 LEVERONI CT. #101 Novato, CA 94949 |
Product Code | EKS |
CFR Regulation Number | 872.4565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-04-18 |
Decision Date | 1989-09-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DENTAL PIK 77280337 not registered Dead/Abandoned |
Igor Sobolev 2007-09-14 |
DENTAL PIK 76497459 not registered Dead/Abandoned |
U.S. DenTek Corporation 2003-03-14 |
DENTAL PIK 73741611 not registered Dead/Abandoned |
U.S. DENTEK CORPORATION 1988-07-22 |
DENTAL PIK 73433983 not registered Dead/Abandoned |
U.S. DENTEK CORPORATION 1983-06-30 |