Inspirease

FDA 510(k) K832037 · Key Pharmaceuticals, Inc.

Substantially Equivalent

510(k) numberK832037

Submission

Device name
Inspirease
Applicant
Key Pharmaceuticals, Inc.
Kenilworth, NJ, US
Received
June 24, 1983
Decision date
August 16, 1983
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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More from Medical Industries America, Inc.

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Questions and answers

When was Inspirease cleared by the FDA?

Inspirease (K832037) received a 510(k) decision of Substantially Equivalent on August 16, 1983, 53 days after the submission was received.

What is the product code of K832037?

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