RESUSCITATION BAG EXHALATION FILTER
K-Number: K883693 · 1988-09-30
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Device Summary
Frequently Asked Questions
What is the RESUSCITATION BAG EXHALATION FILTER?
RESUSCITATION BAG EXHALATION FILTER 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 K883693.
When did RESUSCITATION BAG EXHALATION FILTER receive FDA 510(k) clearance?
RESUSCITATION BAG EXHALATION FILTER received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883693.
Who is the listed applicant for RESUSCITATION BAG EXHALATION FILTER?
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 RESUSCITATION BAG EXHALATION FILTER?
The FDA product code for RESUSCITATION BAG EXHALATION FILTER is CAH.
Related Clinical Trials
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.
Other records listing Intertech Resources, 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.
Related Devices (Code: CAH)
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.
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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