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FDA 510(k)

THE KEEPER

K-Number: K870803 · 1987-05-06

ApplicantThe Keeper Co.
Decision Date1987-05-06
Product CodeHHE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE KEEPER is the device name listed in this FDA 510(k) record. The listed applicant is The Keeper Co.. It received FDA 510(k) clearance on 1987-05-06 under 510(k) number K870803. The device is classified under product code HHE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE KEEPER?

THE KEEPER is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is The Keeper Co.. The 510(k) number is K870803.

When did THE KEEPER receive FDA 510(k) clearance?

THE KEEPER received FDA 510(k) clearance on 1987-05-06, under 510(k) number K870803.

Who is the listed applicant for THE KEEPER?

The FDA 510(k) record lists The Keeper Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE KEEPER?

The FDA product code for THE KEEPER is HHE.

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Related Devices (Code: HHE)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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