Device Labs, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Device Labs, Inc. makes
Device Labs, Inc. makes implantable drug delivery systems, including the CHEMOSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM and related variants, as well as intravascular administration sets, percutaneous introducer kits, and LO-CORE needles.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Chemosite(Tm) Implantable Drug Delivery System Ref K901722
Regimes: 510(k) Registry: 510(k)Chemosite Implantable Drug Delivery Ref K930632
Regimes: 510(k) Registry: 510(k)Intravascular Administration Set Ref K883764
Regimes: 510(k) Registry: 510(k)Percutaneous Introducer Kit Ref K902135
Regimes: 510(k) Registry: 510(k)Lo-Core Needle Ref K882064
Regimes: 510(k) Registry: 510(k)Chemosite Implantable Drug Delivery System Ref K904417
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Device Labs, Inc. have in the registry?
The registry currently lists 6 devices for Device Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Device Labs, Inc.'s devices?
Among its 6 most recently registered devices, Device Labs, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Device Labs, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Device Labs, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Device Labs, Inc. in the registry?
The most recently registered devices listed for Device Labs, Inc. include CHEMOSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM, CHEMOSITE IMPLANTABLE DRUG DELIVERY, INTRAVASCULAR ADMINISTRATION SET and PERCUTANEOUS INTRODUCER KIT.