Monaghan Aerochamber with Mask

FDA 510(k) K874513 · Monaghan Medical Corp.

Substantially Equivalent

510(k) numberK874513

Submission

Device name
Monaghan Aerochamber with Mask
Applicant
Monaghan Medical Corp.
Plattsburgh, NY, US
Received
November 2, 1987
Decision date
December 30, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CCQ – Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Device class
Class I (low risk)
Regulation
21 CFR 868.5640
Specialty
Anesthesiology

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K895115Frank Inhaler Thermal SCCQ · Traditional Buttner-Frank GmbH05/18/1990SE
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Questions and answers

When was Monaghan Aerochamber with Mask cleared by the FDA?

Monaghan Aerochamber with Mask (K874513) received a 510(k) decision of Substantially Equivalent on December 30, 1987, 58 days after the submission was received.

What is the product code of K874513?

The FDA product code is CCQ – Nebulizer, Medicinal, Non-Ventilatory (Atomizer), a Class I (low risk) device regulated under 21 CFR 868.5640.