Device Labs, Inc.
6 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| CHEMOSITE IMPLANTABLE DRUG DELIVERY (K930632) | Device Labs, Inc. | 1993-12-22 |
| CHEMOSITE IMPLANTABLE DRUG DELIVERY SYSTEM (K904417) | Device Labs, Inc. | 1990-12-05 |
| PERCUTANEOUS INTRODUCER KIT (K902135) | Device Labs, Inc. | 1990-08-01 |
| CHEMOSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM (K901722) | Device Labs, Inc. | 1990-07-03 |
| INTRAVASCULAR ADMINISTRATION SET (K883764) | Device Labs, Inc. | 1988-12-19 |
| LO-CORE NEEDLE (K882064) | Device Labs, Inc. | 1988-07-08 |
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Every clearance here is in the API, with alerts when new ones post.