FDA 510(k) Applications Submitted by DERLIN COMPANY LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964817 | 11/29/1996 | DERLIN | DERLIN COMPANY LTD. |
| K974223 | 11/12/1997 | NITRILE, POWDER FREE, POLY COATED PATIENT EXAMINATION GLOVES | DERLIN COMPANY LTD. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact