The following data is part of a premarket notification filed by Med-tool, Inc. with the FDA for Vice Or Bench Vice.
Device ID | K872385 |
510k Number | K872385 |
Device Name: | VICE OR BENCH VICE |
Classification | Vise, Bench, Surgical |
Applicant | MED-TOOL, INC. 12434 MATTHEWS LN. St. Louis, MO 63127 |
Contact | Mayerik, Jr. |
Correspondent | Mayerik, Jr. MED-TOOL, INC. 12434 MATTHEWS LN. St. Louis, MO 63127 |
Product Code | LSA |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-19 |
Decision Date | 1987-07-16 |