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FDA 510(k)

PRECISION MEDICAL DISPOSABLE HUMIDIFIER

K-Number: K902970 · 1990-08-14

ApplicantPrecision Medical, Inc.
Decision Date1990-08-14
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION MEDICAL DISPOSABLE HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 1990-08-14 under 510(k) number K902970. 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 PRECISION MEDICAL DISPOSABLE HUMIDIFIER?

PRECISION MEDICAL DISPOSABLE HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Precision Medical, Inc.. The 510(k) number is K902970.

When did PRECISION MEDICAL DISPOSABLE HUMIDIFIER receive FDA 510(k) clearance?

PRECISION MEDICAL DISPOSABLE HUMIDIFIER received FDA 510(k) clearance on 1990-08-14, under 510(k) number K902970.

Who is the listed applicant for PRECISION MEDICAL DISPOSABLE HUMIDIFIER?

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

What is the FDA product code for PRECISION MEDICAL DISPOSABLE HUMIDIFIER?

The FDA product code for PRECISION MEDICAL DISPOSABLE HUMIDIFIER is BTT.

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Other records listing Precision 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.

K173807Accu O2 Oxygen AnalyzerK103563PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150K103324PRECISION LIQUID OXYGEN SYSTEMK090781HELIO2 BLENDERK072348PRECISION OXYGEN CONCENTRATORK063096PRECISION OXYGEN MONITOR

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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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