Holopack International, LP
United StatesFDA applicant, unverified
- Devices
- 3
What Holopack International, LP makes
Holopack International, LP manufactures inhalation solutions, including sterile 0.9% sodium chloride inhalation solution, USP, sodium chloride inhalation solution, USP, and sterile water for inhalation, USP. These products are designed for respiratory therapy and nebulization procedures.
The company’s portfolio is regulated under FDA’s Class II medical device classification, with devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
0.9.% Sodium Chloride Inhalation Solution, Usp Ref K974056
Regimes: 510(k) Registry: 510(k)Sodium Chloride Inhalation Solution, Usp Ref K972466
Regimes: 510(k) Registry: 510(k)Sterile Water For Inhalation, Usp Ref K972467
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Holopack International, LP have in the registry?
The registry currently lists 3 devices for Holopack International, LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list Holopack International, LP's devices?
Among its 3 most recently registered devices, Holopack International, LP has devices listed in FDA 510(k) (3 devices).
What risk classes do Holopack International, LP's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Holopack International, LP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Holopack International, LP in the registry?
The most recently registered devices listed for Holopack International, LP include 0.9.% SODIUM CHLORIDE INHALATION SOLUTION, USP, SODIUM CHLORIDE INHALATION SOLUTION, USP and STERILE WATER FOR INHALATION, USP.