Clk Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Clk Intl., Inc. makes
Clk Intl., Inc. manufactures single-use protective barriers for medical devices, including latex probe covers for ultrasound and examination gloves. These products are designed to reduce contamination risk during procedures by providing a sterile barrier over probes and hands.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Clk Int'l Powder Free Latex Examination Glove Ref K974371
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clk Intl., Inc. have in the registry?
The registry currently lists 2 devices for Clk Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clk Intl., Inc.'s devices?
Among its 2 most recently registered devices, Clk Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Clk Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clk Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clk Intl., Inc. in the registry?
The most recently registered devices listed for Clk Intl., Inc. include CLK INT'L. SANITARY LATEX PROBE COVER, CLK ULTRASOUND PROBE COVER and CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE.