FDA 510(k) Applications Submitted by TSK LABORATORY, JAPAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970370 | 01/31/1997 | TSK STERIJEKT PREMIUM DISPOSABLE HYPODERMIC NEEDLE | TSK LABORATORY, JAPAN |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact