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FDA 510(k)

MEMBRANE HUMIDIFIER

K-Number: K873472 · 1988-01-19

ApplicantRespiratory Support Products, Inc.
Decision Date1988-01-19
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEMBRANE HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K873472. 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 MEMBRANE HUMIDIFIER?

MEMBRANE HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K873472.

When did MEMBRANE HUMIDIFIER receive FDA 510(k) clearance?

MEMBRANE HUMIDIFIER received FDA 510(k) clearance on 1988-01-19, under 510(k) number K873472.

Who is the listed applicant for MEMBRANE HUMIDIFIER?

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

What is the FDA product code for MEMBRANE HUMIDIFIER?

The FDA product code for MEMBRANE HUMIDIFIER is BTT.

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Other records listing Respiratory Support Products, 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.

K983862CLOUD 1 HUMIDIFICATION SYSTEMK921190ADAP-TEMP TEMPERATURE SENSOR ADAPTERK920469MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIEK921510GAS SAMPLING KIT MODIFICATIONK913082BI-TEMP TEMPERATURE MONITOR,MODEL TM-300DK912280BI-TEMP TEMPERATURE MONITOR, MODEL TM-400D

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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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