Acutek Adhesive Specialties, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Acutek's Hydrocolloid Wound Dressing, Tib 197012 Ref K974892
Regimes: 510(k) Registry: 510(k)Acutek's Clearpasage Ref K962698
Regimes: 510(k) Registry: 510(k)Transparent Dressing Ref K943111
Regimes: 510(k) Registry: 510(k)Acutek's Clearpassage Ref K951644
Regimes: 510(k) Registry: 510(k)Acutek's Hydrocolloid Wound Dressing, Tib 997002 Ref K974890
Regimes: 510(k) Registry: 510(k)Acutek's Hydrocolloid Wound Dressing, Tib 197013 Ref K974891
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acutek Adhesive Specialties, Inc. have in the registry?
The registry currently lists 6 devices for Acutek Adhesive Specialties, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acutek Adhesive Specialties, Inc.'s devices?
Among its 6 most recently registered devices, Acutek Adhesive Specialties, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Acutek Adhesive Specialties, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Acutek Adhesive Specialties, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Acutek Adhesive Specialties, Inc. in the registry?
The most recently registered devices listed for Acutek Adhesive Specialties, Inc. include ACUTEK'S HYDROCOLLOID WOUND DRESSING, TIB 197012, ACUTEK'S CLEARPASAGE, TRANSPARENT DRESSING and ACUTEK'S CLEARPASSAGE.