Dr. Boo Co., Ltd.
Also registered as Dr.Boo Company Limited
Country not established
- Devices
- 5
Catalogue
Patient Examination Glove (Latex) Ref K891271
510(k) 510(k)- 510(k) 510(k)
Dr. Boo Powder-Free Latex Exam Gloves Ref K941240
510(k) 510(k)Patient Examination Gloves (Latex) Ref K891242
510(k) 510(k)Patient Examination Gloves Ref K891313
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Boo Co., Ltd. have in the registry?
The registry currently lists 5 devices for Dr. Boo Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Boo Co., Ltd.'s devices?
Among its 5 most recently registered devices, Dr. Boo Co., Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Dr. Boo Co., Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dr. Boo Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Boo Co., Ltd. in the registry?
The most recently registered devices listed for Dr. Boo Co., Ltd. include PATIENT EXAMINATION GLOVE (LATEX), Proclean - Nitrile Powder Free Examination Gloves, DR. BOO POWDER-FREE LATEX EXAM GLOVES and PATIENT EXAMINATION GLOVES (LATEX).