Glasrock Plastics, Inc.
Country not established
- Devices
- 1
What Glasrock Plastics, Inc. makes
Glasrock Plastics, Inc. manufactures blood serum filters designed for laboratory filtration applications, specifically the Filter Sampler Blood Serum Filter. These devices are intended for use in processing and preparing blood serum samples for analysis.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The products are listed in the FDA’s 510(k) database. Glasrock Plastics, Inc. is based in the United States.
Catalogue
Filter Sampler Blood Serum Filter Ref K811036
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glasrock Plastics, Inc. have in the registry?
The registry currently lists 1 device for Glasrock Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glasrock Plastics, Inc.'s devices?
Among its 1 most recently registered device, Glasrock Plastics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Glasrock Plastics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Glasrock Plastics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glasrock Plastics, Inc. in the registry?
The most recently registered devices listed for Glasrock Plastics, Inc. include FILTER SAMPLER BLOOD SERUM FILTER.