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)

CONDOM TAKASO RUBBER PRODUCTS SDN/BDH

K-Number: K871036 · 1987-10-20

Decision Date1987-10-20
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONDOM TAKASO RUBBER PRODUCTS SDN/BDH is the device name listed in this FDA 510(k) record. The listed applicant is Takaso Rubber C/O Interstate Supplier, Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K871036. 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 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.

↑