The following data is part of a premarket notification filed by Inman Medical Corp. with the FDA for Shur-grip.
Device ID | K912834 |
510k Number | K912834 |
Device Name: | SHUR-GRIP |
Classification | Instrument, Surgical, Disposable |
Applicant | INMAN MEDICAL CORP. P.O. BOX 171077 Arlington, TX 76003 |
Contact | Clay Wilson |
Correspondent | Clay Wilson INMAN MEDICAL CORP. P.O. BOX 171077 Arlington, TX 76003 |
Product Code | KDC |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-26 |
Decision Date | 1991-07-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SHUR-GRIP 78196118 2913839 Dead/Cancelled |
NEWELL OPERATING COMPANY 2002-12-19 |
SHUR-GRIP 77154772 3371832 Live/Registered |
AQSEPTENCE GROUP, INC. 2007-04-12 |
SHUR-GRIP 75154895 2231333 Dead/Cancelled |
U.S. Netting, Inc. 1996-08-23 |
SHUR-GRIP 73835878 not registered Dead/Abandoned |
CENTRAL STATES DIVERSIFIED, INC. 1989-11-03 |
SHUR-GRIP 72147640 0756088 Dead/Expired |
STANDARD CORRUGATED CASE CORP. 1962-06-25 |
SHUR-GRIP 72147639 0755746 Dead/Expired |
STANDARD CORRUGATED CASE CORP. 1962-06-25 |