E-CLIP

Electrode, Pacemaker, Temporary

The following data is part of a premarket notification filed by Joel Cohen & Esther R. Cohen with the FDA for E-clip.

Device ID	K900982
510k Number	K900982
Device Name:	E-CLIP
Classification	Electrode, Pacemaker, Temporary
Applicant	JOEL COHEN & ESTHER R. COHEN 1020 NW 99TH AVE. Plantation, FL 33322
Contact	Joel Cohen
Correspondent	Joel Cohen JOEL COHEN & ESTHER R. COHEN 1020 NW 99TH AVE. Plantation, FL 33322
Product Code	LDF
CFR Regulation Number	870.3680 [🔎]
Decision	Substantially Equivalent (SESE)
Type	Traditional
3rd Party Reviewed	No
Combination Product	No
Date Received	1990-03-02
Decision Date	1990-04-19

Mark Image Registration \| Serial	Company Trademark Application Date
E-CLIP 98215471 not registered Live/Pending	Envision Building Products LLC 2023-10-09
E-CLIP 78675110 not registered Dead/Abandoned	ROYAL CONSUMER INFORMATION PRODUCTS, INC. 2005-07-21
E-CLIP 78638974 not registered Dead/Abandoned	Pursuit Marketing, Inc. 2005-05-27
E-CLIP 77717135 not registered Dead/Abandoned	Milburn, Mark 2009-04-20
E-CLIP 75856450 2733513 Dead/Cancelled	Hummingbird Communications Ltd. 1999-11-23
E-CLIP 75777591 not registered Dead/Abandoned	eCommercial.com, Inc. 1999-08-18
E-CLIP 74124809 1746420 Dead/Cancelled	COEHN, ESTHER 1990-12-19
E-CLIP 74124809 1746420 Dead/Cancelled	COHEN, ESTHER 1990-12-19