Pacific Rim Products, Inc.
AustraliaFDA applicant, unverified
- Devices
- 1
What Pacific Rim Products, Inc. makes
Pacific Rim Products, Inc. manufactures the MINI-LANCET, a single-use device designed for blood sampling, typically used in glucose monitoring and other diagnostic procedures.
The MINI-LANCET is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Mini-Lancet Ref K931481
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pacific Rim Products, Inc. have in the registry?
The registry currently lists 1 device for Pacific Rim Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pacific Rim Products, Inc.'s devices?
Among its 1 most recently registered device, Pacific Rim Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pacific Rim Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pacific Rim Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pacific Rim Products, Inc. in the registry?
The most recently registered devices listed for Pacific Rim Products, Inc. include MINI-LANCET.