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FDA 510(k)

STERILE INHALATION WATER TRANSFER SET

K-Number: K882582 · 1988-09-30

ApplicantIntertech Resources, Inc.
Decision Date1988-09-30
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STERILE INHALATION WATER TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1988-09-30 under 510(k) number K882582. 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 STERILE INHALATION WATER TRANSFER SET?

STERILE INHALATION WATER TRANSFER SET is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K882582.

When did STERILE INHALATION WATER TRANSFER SET receive FDA 510(k) clearance?

STERILE INHALATION WATER TRANSFER SET received FDA 510(k) clearance on 1988-09-30, under 510(k) number K882582.

Who is the listed applicant for STERILE INHALATION WATER TRANSFER SET?

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

What is the FDA product code for STERILE INHALATION WATER TRANSFER SET?

The FDA product code for STERILE INHALATION WATER TRANSFER SET is BTT.

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Other records listing Intertech Resources, Inc. as applicant

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Related Devices (Code: BTT)

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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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