Exerciser, Air-Eze Incentive

FDA 510(k) K781833 · Chesebrough-Pond'S U.S.A. Co.

Substantially Equivalent

510(k) numberK781833

Submission

Device name
Exerciser, Air-Eze Incentive
Applicant
Chesebrough-Pond'S U.S.A. Co.
Mchenry, IL, US
Received
October 30, 1978
Decision date
November 14, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BWF – Spirometer, Therapeutic (Incentive)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5690
Specialty
Anesthesiology

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K844186Continent Stoma System & AccessoriesKBG · Traditional 01/15/1985SE
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Questions and answers

When was Exerciser, Air-Eze Incentive cleared by the FDA?

Exerciser, Air-Eze Incentive (K781833) received a 510(k) decision of Substantially Equivalent on November 14, 1978, 15 days after the submission was received.

What is the product code of K781833?

The FDA product code is BWF – Spirometer, Therapeutic (Incentive), a Class II (moderate risk) device regulated under 21 CFR 868.5690.