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FDA 510(k)

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION

K-Number: K062091 · 2006-08-08

ApplicantPorous Media Corp.
Decision Date2006-08-08
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Porous Media Corp.. It received FDA 510(k) clearance on 2006-08-08 under 510(k) number K062091. 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 POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION?

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION is a medical device that received FDA 510(k) clearance on 2006-08-08. The listed applicant is Porous Media Corp.. The 510(k) number is K062091.

When did POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION receive FDA 510(k) clearance?

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION received FDA 510(k) clearance on 2006-08-08, under 510(k) number K062091.

Who is the listed applicant for POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION?

The FDA 510(k) record lists Porous Media Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION?

The FDA product code for POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION is BTT.

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Other records listing Porous Media 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.

K061426OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTERK982385POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTERK982127POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTERK965020POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTERK964979POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER

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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

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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