AEROCHAMBER
K-Number: K872037 · 1987-07-24
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Device Summary
Frequently Asked Questions
What is the AEROCHAMBER?
AEROCHAMBER is a medical device that received FDA 510(k) clearance on 1987-07-24. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K872037.
When did AEROCHAMBER receive FDA 510(k) clearance?
AEROCHAMBER received FDA 510(k) clearance on 1987-07-24, under 510(k) number K872037.
Who is the listed applicant for AEROCHAMBER?
The FDA 510(k) record lists Monaghan Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEROCHAMBER?
The FDA product code for AEROCHAMBER is BYP.
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 Monaghan Medical Corp. 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: BYP)
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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