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FDA 510(k)

INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT

K-Number: K896923 · 1990-03-12

ApplicantIntertech Resources, Inc.
Decision Date1990-03-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent for Some Indications

Device Summary

INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT 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 1990-03-12 under 510(k) number K896923. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT?

INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT is a medical device that received FDA 510(k) clearance on 1990-03-12. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K896923.

When did INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT receive FDA 510(k) clearance?

INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT received FDA 510(k) clearance on 1990-03-12, under 510(k) number K896923.

Who is the listed applicant for INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT?

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 INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT?

The FDA product code for INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT is CAF.

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Other records listing Intertech Resources, Inc. as applicant

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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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