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)

CONDOMS

K-Number: K880819 · 1989-08-11

Decision Date1989-08-11
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is Universal Trade, Inc.. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K880819. 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 CONDOMS?

CONDOMS is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Universal Trade, Inc.. The 510(k) number is K880819.

When did CONDOMS receive FDA 510(k) clearance?

CONDOMS received FDA 510(k) clearance on 1989-08-11, under 510(k) number K880819.

Who is the listed applicant for CONDOMS?

The FDA 510(k) record lists Universal Trade, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONDOMS?

The FDA product code for CONDOMS 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.

↑