CONDOM TAKASO RUBBER PRODUCTS SDN/BDH
K-Number: K871036 · 1987-10-20
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Device Summary
Frequently Asked Questions
What is the CONDOM TAKASO RUBBER PRODUCTS SDN/BDH?
CONDOM TAKASO RUBBER PRODUCTS SDN/BDH is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Takaso Rubber C/O Interstate Supplier, Inc.. The 510(k) number is K871036.
When did CONDOM TAKASO RUBBER PRODUCTS SDN/BDH receive FDA 510(k) clearance?
CONDOM TAKASO RUBBER PRODUCTS SDN/BDH received FDA 510(k) clearance on 1987-10-20, under 510(k) number K871036.
Who is the listed applicant for CONDOM TAKASO RUBBER PRODUCTS SDN/BDH?
The FDA 510(k) record lists Takaso Rubber C/O Interstate Supplier, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONDOM TAKASO RUBBER PRODUCTS SDN/BDH?
The FDA product code for CONDOM TAKASO RUBBER PRODUCTS SDN/BDH 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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