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 |
| K250284 | 01/31/2025 | TSK SELECTÖ Needle | TSK Laboratory, Japan |
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