The following data is part of a premarket notification filed by Ametek with the FDA for Dynamometer - Model Fce And Model Msc.
| Device ID | K042889 |
| 510k Number | K042889 |
| Device Name: | DYNAMOMETER - MODEL FCE AND MODEL MSC |
| Classification | Dynamometer, Ac-powered |
| Applicant | AMETEK 8600 SOMERSET DR. Largo, FL 33773 |
| Contact | Philip Lachance |
| Correspondent | Philip Lachance AMETEK 8600 SOMERSET DR. Largo, FL 33773 |
| Product Code | LBB |
| CFR Regulation Number | 888.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-10-19 |
| Decision Date | 2004-11-16 |
| Summary: | summary |