The following data is part of a premarket notification filed by Medical Components, Inc. with the FDA for Mcsc6ps Medical Components.
| Device ID | K821820 |
| 510k Number | K821820 |
| Device Name: | MCSC6PS MEDICAL COMPONENTS |
| Classification | Instrument, Ultrasonic Surgical |
| Applicant | MEDICAL COMPONENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LFL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-21 |
| Decision Date | 1982-07-13 |