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FDA 510(k)

WORLD'S BEST (CONTRACEPTIVE)

K-Number: K820564 · 1982-05-28

Decision Date1982-05-28
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WORLD'S BEST (CONTRACEPTIVE) is the device name listed in this FDA 510(k) record. The listed applicant is Rosen Kilde Stenhoj. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K820564. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORLD'S BEST (CONTRACEPTIVE)?

WORLD'S BEST (CONTRACEPTIVE) is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Rosen Kilde Stenhoj. The 510(k) number is K820564.

When did WORLD'S BEST (CONTRACEPTIVE) receive FDA 510(k) clearance?

WORLD'S BEST (CONTRACEPTIVE) received FDA 510(k) clearance on 1982-05-28, under 510(k) number K820564.

Who is the listed applicant for WORLD'S BEST (CONTRACEPTIVE)?

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

What is the FDA product code for WORLD'S BEST (CONTRACEPTIVE)?

The FDA product code for WORLD'S BEST (CONTRACEPTIVE) is HIS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HIS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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