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FDA 510(k)

INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR

K-Number: K870253 · 1987-03-06

ApplicantIntertech Resources, Inc.
Decision Date1987-03-06
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR 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 1987-03-06 under 510(k) number K870253. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR?

INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K870253.

When did INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR receive FDA 510(k) clearance?

INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870253.

Who is the listed applicant for INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR?

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 INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR?

The FDA product code for INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR is CBP.

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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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