Solopak Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Solopak Laboratories, Inc. makes
Solopak Laboratories, Inc. manufactures sterile empty vials designed for pharmaceutical use, intended to contain liquid medications or injectable solutions in clinical or manufacturing settings.
These products are regulated under the FDA’s 510(k) clearance pathway as Class II medical devices and are listed in the U.S. regulatory database. The company operates from its base in the United States.
Catalogue
Heparin Lock Flush Solution Usp Kit, 100 Ref K841306
Regimes: 510(k) Registry: 510(k)Heparin Lock Flush Solution Usp Kit Ref K841305
Regimes: 510(k) Registry: 510(k)Max-I-Probe Handpiece Ref K851944
Regimes: 510(k) Registry: 510(k)Heparin Lock Flush Procedure Pack Ref K841166
Regimes: 510(k) Registry: 510(k)Solopak Pharmaceuticals Inc. Sterile Empty Vial Ref K950822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Solopak Laboratories, Inc. have in the registry?
The registry currently lists 5 devices for Solopak Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solopak Laboratories, Inc.'s devices?
Among its 5 most recently registered devices, Solopak Laboratories, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Solopak Laboratories, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Solopak Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solopak Laboratories, Inc. in the registry?
The most recently registered devices listed for Solopak Laboratories, Inc. include HEPARIN LOCK FLUSH SOLUTION USP KIT, 100, HEPARIN LOCK FLUSH SOLUTION USP KIT, MAX-I-PROBE HANDPIECE and HEPARIN LOCK FLUSH PROCEDURE PACK.