The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Lancer Specimen Container.
| Device ID | K792156 |
| 510k Number | K792156 |
| Device Name: | LANCER SPECIMEN CONTAINER |
| Classification | Container, Specimen, Sterile |
| Applicant | SHERWOOD MEDICAL CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FMH |
| CFR Regulation Number | 864.3250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-29 |
| Decision Date | 1979-12-10 |