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FDA 510(k)

VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC

K-Number: K860874 · 1986-03-19

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1986-03-19
Product CodeBYF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTURI MASK W/HUMDIFICATION CUP 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 1986-03-19 under 510(k) number K860874. 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 W/HUMDIFICATION CUP ADULT/PAEDIATRIC?

VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC is a medical device that received FDA 510(k) clearance on 1986-03-19. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K860874.

When did VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC receive FDA 510(k) clearance?

VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860874.

Who is the listed applicant for VENTURI MASK W/HUMDIFICATION CUP 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 W/HUMDIFICATION CUP ADULT/PAEDIATRIC?

The FDA product code for VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC is BYF.

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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.

K883988NON-REBREATHING TEE PIECE (NRTP)K881935MICROCIRRUS MEDICAL NEBULIZERK881178CUFFCHECKK873498INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBINGK874047ASTHMAKITK873447DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR

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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.

K955483TRACH MASK MODEL (245, 246)Hospitak, Inc.K951652VENTIMASK MK IVFlexicare Medical, Ltd.K894457CARNATION TRACHEOSTOMY MASKSDadsun Corp., Ltd.K860873VENTURI MASK/ADULT & PAEDIATRICDhd Medical Products Div. Diemolding Corp.K852618OXY-DIALAshai Co. , Ltd.K832725DUAL DIAL VENTURI STYLE MASKAirlife, Inc.

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.

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