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FDA 510(k)

EXERCISER, AIR-EZE INCENTIVE

K-Number: K781833 · 1978-11-14

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1978-11-14
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EXERCISER, AIR-EZE INCENTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1978-11-14 under 510(k) number K781833. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXERCISER, AIR-EZE INCENTIVE?

EXERCISER, AIR-EZE INCENTIVE is a medical device that received FDA 510(k) clearance on 1978-11-14. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K781833.

When did EXERCISER, AIR-EZE INCENTIVE receive FDA 510(k) clearance?

EXERCISER, AIR-EZE INCENTIVE received FDA 510(k) clearance on 1978-11-14, under 510(k) number K781833.

Who is the listed applicant for EXERCISER, AIR-EZE INCENTIVE?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXERCISER, AIR-EZE INCENTIVE?

The FDA product code for EXERCISER, AIR-EZE INCENTIVE is BWF.

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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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