RIA (CONDOM)
K-Number: K895091 · 1990-01-16
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Device Summary
Frequently Asked Questions
What is the RIA (CONDOM)?
RIA (CONDOM) is a medical device that received FDA 510(k) clearance on 1990-01-16. The listed applicant is La Technology Sdn. Bhd.. The 510(k) number is K895091.
When did RIA (CONDOM) receive FDA 510(k) clearance?
RIA (CONDOM) received FDA 510(k) clearance on 1990-01-16, under 510(k) number K895091.
Who is the listed applicant for RIA (CONDOM)?
The FDA 510(k) record lists La Technology Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIA (CONDOM)?
The FDA product code for RIA (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.
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