RUBBER CONTRACEPTIVE (CONDOM)
K-Number: K896142 · 1990-06-06
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Device Summary
Frequently Asked Questions
What is the RUBBER CONTRACEPTIVE (CONDOM)?
RUBBER CONTRACEPTIVE (CONDOM) is a medical device that received FDA 510(k) clearance on 1990-06-06. The listed applicant is Guangzhou No. 11 Rubber Factory. The 510(k) number is K896142.
When did RUBBER CONTRACEPTIVE (CONDOM) receive FDA 510(k) clearance?
RUBBER CONTRACEPTIVE (CONDOM) received FDA 510(k) clearance on 1990-06-06, under 510(k) number K896142.
Who is the listed applicant for RUBBER CONTRACEPTIVE (CONDOM)?
The FDA 510(k) record lists Guangzhou No. 11 Rubber Factory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUBBER CONTRACEPTIVE (CONDOM)?
The FDA product code for RUBBER CONTRACEPTIVE (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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