Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BILLY BOY MALE LATEX CONDOM

K-Number: K103119 · 2011-02-24

Decision Date2011-02-24
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BILLY BOY MALE LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Sheila Pickering PHD. It received FDA 510(k) clearance on 2011-02-24 under 510(k) number K103119. 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 BILLY BOY MALE LATEX CONDOM?

BILLY BOY MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2011-02-24. The listed applicant is Sheila Pickering PHD. The 510(k) number is K103119.

When did BILLY BOY MALE LATEX CONDOM receive FDA 510(k) clearance?

BILLY BOY MALE LATEX CONDOM received FDA 510(k) clearance on 2011-02-24, under 510(k) number K103119.

Who is the listed applicant for BILLY BOY MALE LATEX CONDOM?

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

What is the FDA product code for BILLY BOY MALE LATEX CONDOM?

The FDA product code for BILLY BOY MALE LATEX CONDOM 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

View on FDA Database →

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

↑