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FDA 510(k)

HPD HUMIDIFIER WICK

K-Number: K841851 · 1984-06-05

ApplicantHpd Medical, Inc.
Decision Date1984-06-05
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HPD HUMIDIFIER WICK is the device name listed in this FDA 510(k) record. The listed applicant is Hpd Medical, Inc.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841851. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HPD HUMIDIFIER WICK?

HPD HUMIDIFIER WICK is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Hpd Medical, Inc.. The 510(k) number is K841851.

When did HPD HUMIDIFIER WICK receive FDA 510(k) clearance?

HPD HUMIDIFIER WICK received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841851.

Who is the listed applicant for HPD HUMIDIFIER WICK?

The FDA 510(k) record lists Hpd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HPD HUMIDIFIER WICK?

The FDA product code for HPD HUMIDIFIER WICK is BTT.

Related Clinical Trials

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Other records listing Hpd Medical, Inc. 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.

K914994HPD HEATER BASESK895795HPD TUBING CONNECTORSK885314HPD STERILE HUMIDIFYING CHAMBERK864173HPD HUMIDIFYING CHAMBERK821957CATH-LOK

Related Devices (Code: BTT)

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.

K262268Optiflow Oxygen Kit (AA484J)Fisher and Paykel Healthcare LimitedK254078HVT 2.0Vapotherm, Inc.K251448FL-10000U Respiratory HumidifierFlexicare Medical Limited.K251419Laboratorios Biogalenic Sterile Water for Inhalation, USPLaboratorios Biogalenic S.A. DE C.V.K253479Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)Fisher & Paykel Healthcare, Ltd.K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra SmallMedline Industries, LP

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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