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FDA 510(k)

VENTURI MASK/ADULT & PAEDIATRIC

K-Number: K860873 · 1986-03-20

Decision Date1986-03-20
Product CodeBYF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTURI MASK/ADULT & PAEDIATRIC is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1986-03-20 under 510(k) number K860873. The device is classified under product code BYF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 43 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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