The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Min-identoflex.
Device ID | K873002 |
510k Number | K873002 |
Device Name: | MIN-IDENTOFLEX |
Classification | Disk, Abrasive |
Applicant | CENTRIX, INC. 30 STRAN RD. Milford, CT 06460 |
Contact | John Discko |
Correspondent | John Discko CENTRIX, INC. 30 STRAN RD. Milford, CT 06460 |
Product Code | EHJ |
CFR Regulation Number | 872.6010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-04 |
Decision Date | 1987-08-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MIN-IDENTOFLEX 73180599 1125762 Dead/Cancelled |
CAVITRON CORPORATION 1978-07-24 |