Rd Medical Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Parset, Model A10001E Ref K992104
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rd Medical Mfg., Inc. have in the registry?
The registry currently lists 4 devices for Rd Medical Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rd Medical Mfg., Inc.'s devices?
Among its 4 most recently registered devices, Rd Medical Mfg., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Rd Medical Mfg., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Rd Medical Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rd Medical Mfg., Inc. in the registry?
The most recently registered devices listed for Rd Medical Mfg., Inc. include PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET SECONDARY SECONDARY ADMINISTRATION SET, MODEL A1400, PARSET PRIMARY SET WITH CHECK VALVE, MODEL A10002E, PARSET, MODEL A10001E and PARSET NEEDLELESS PRIMARY SET FOR BLUNT CANNULA, A10003E, PARSET NEEDLELESS SECONDARY SET WITH BLUNT CANNULA, A14003E.