Recto Molded Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Recto Molded Products, Inc. makes
Recto Molded Products, Inc. manufactures manual and powered evacuator/aspirator devices, including the QUINEVAC EVACUATOR/ASPIRATOR and the QUINEVAC II, designed for medical suction applications.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Quinevac Evacuator/Aspirator Ref K920628
Regimes: 510(k) Registry: 510(k)Quinevac Ii Ref K920629
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Recto Molded Products, Inc. have in the registry?
The registry currently lists 2 devices for Recto Molded Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Recto Molded Products, Inc.'s devices?
Among its 2 most recently registered devices, Recto Molded Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Recto Molded Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Recto Molded Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Recto Molded Products, Inc. in the registry?
The most recently registered devices listed for Recto Molded Products, Inc. include QUINEVAC EVACUATOR/ASPIRATOR and QUINEVAC II.