New York Blood Center, Inc.
Country not established
- Devices
- 1
What New York Blood Center, Inc. makes
The New York Blood Center, Inc. manufactures the MEL-PAK General Drug Delivery System Kit, a sterile, single-use system designed for intravenous drug administration, including blood and blood component transfusions.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Mel-Pak General Drug Delivery System Kit Ref K894787
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New York Blood Center, Inc. have in the registry?
The registry currently lists 1 device for New York Blood Center, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list New York Blood Center, Inc.'s devices?
Among its 1 most recently registered device, New York Blood Center, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do New York Blood Center, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for New York Blood Center, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New York Blood Center, Inc. in the registry?
The most recently registered devices listed for New York Blood Center, Inc. include MEL-PAK GENERAL DRUG DELIVERY SYSTEM KIT.