Peter F. Lee, Inc.
Country not established
- Devices
- 1
What Peter F. Lee, Inc. makes
Peter F. Lee, Inc. manufactures LEE syringes, which are single-use, pre-filled or disposable syringes designed for accurate medication delivery in clinical and homecare settings.
The company’s syringes are regulated under the FDA’s 510(k) pathway as Class II devices and are listed in the U.S. Food and Drug Administration’s database. The manufacturer is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lee Syringe Ref K842371
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peter F. Lee, Inc. have in the registry?
The registry currently lists 1 device for Peter F. Lee, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peter F. Lee, Inc.'s devices?
Among its 1 most recently registered device, Peter F. Lee, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Peter F. Lee, Inc. in the registry?
The most recently registered devices listed for Peter F. Lee, Inc. include LEE SYRINGE.