Bradstreet Clinical Research Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Bradstreet Clinical Research Assoc., Inc. makes
Bradstreet Clinical Research Assoc., Inc. manufactures single-use contact lens cases, including the Ryder Contact Lens Case and its Model 10670 variant, as well as the Flutter and Flutter D devices, which appear to be reusable or disposable diagnostic tools for ophthalmic use.
These products are classified as Class II medical devices in the US and are listed under the FDA’s 510(k) pathway. The company operates within the regulatory framework of the United States.
Catalogue
Flutter(R) Ref K946083
Regimes: 510(k) Registry: 510(k)Ryder Contact Lens Case Ref K951181
Regimes: 510(k) Registry: 510(k)Ryder Contact Lens Case Model 10670 Ref K951182
Regimes: 510(k) Registry: 510(k)Flutter D Ref K972859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bradstreet Clinical Research Assoc., Inc. have in the registry?
The registry currently lists 4 devices for Bradstreet Clinical Research Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bradstreet Clinical Research Assoc., Inc.'s devices?
Among its 4 most recently registered devices, Bradstreet Clinical Research Assoc., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Bradstreet Clinical Research Assoc., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bradstreet Clinical Research Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bradstreet Clinical Research Assoc., Inc. in the registry?
The most recently registered devices listed for Bradstreet Clinical Research Assoc., Inc. include FLUTTER(R), RYDER CONTACT LENS CASE, RYDER CONTACT LENS CASE MODEL 10670 and FLUTTER D.