VENTURI MASK/ADULT & PAEDIATRIC
K-Number: K860873 · 1986-03-20
Advertisement
Device Summary
Frequently Asked Questions
What is the VENTURI MASK/ADULT & PAEDIATRIC?
VENTURI MASK/ADULT & PAEDIATRIC is a medical device that received FDA 510(k) clearance on 1986-03-20. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K860873.
When did VENTURI MASK/ADULT & PAEDIATRIC receive FDA 510(k) clearance?
VENTURI MASK/ADULT & PAEDIATRIC received FDA 510(k) clearance on 1986-03-20, under 510(k) number K860873.
Who is the listed applicant for VENTURI MASK/ADULT & PAEDIATRIC?
The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENTURI MASK/ADULT & PAEDIATRIC?
The FDA product code for VENTURI MASK/ADULT & PAEDIATRIC is BYF.
Related Clinical Trials
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.
Other records listing Dhd Medical Products Div. Diemolding Corp. 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: BYF)
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.
Advertisement