PNEUMOCLEAR
K-Number: K170784 · 2017-05-15
Device Summary
Frequently Asked Questions
What is the PNEUMOCLEAR?
PNEUMOCLEAR is a medical device that received FDA 510(k) clearance on 2017-05-15. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K170784.
When did PNEUMOCLEAR receive FDA 510(k) clearance?
PNEUMOCLEAR received FDA 510(k) clearance on 2017-05-15, under 510(k) number K170784.
Who is the listed applicant for PNEUMOCLEAR?
The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PNEUMOCLEAR?
The FDA product code for PNEUMOCLEAR is HIF.
Other records listing W.O.M. World of Medicine GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HIF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.