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)

LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE

K-Number: K893217 · 1990-01-10

ApplicantShinhen Corp.
Decision Date1990-01-10
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Shinhen Corp.. It received FDA 510(k) clearance on 1990-01-10 under 510(k) number K893217. 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 LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE?

LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE is a medical device that received FDA 510(k) clearance on 1990-01-10. The listed applicant is Shinhen Corp.. The 510(k) number is K893217.

When did LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE receive FDA 510(k) clearance?

LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE received FDA 510(k) clearance on 1990-01-10, under 510(k) number K893217.

Who is the listed applicant for LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE?

The FDA 510(k) record lists Shinhen Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE?

The FDA product code for LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K262108FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male Latex Condoms – Aqueous Lubricant (Plain);FAMA Male Latex Condoms – Aqueous Lubricant (Ribbed);FAMA Male Latex Condoms – Aqueous Lubricant (Dotted);FAMA Male Latex Condoms – Aqueous Lubricant (Non-regular Shaped);MO Male Latex Condoms – Aqueous Lubricant (Ultra-thin);MO Male Latex Condoms – Aqueous Lubricant (Plain);MO Male Latex Condoms – Aqueous Lubricant (Ribbed);MO Male Latex Condoms – Aqueous Lubricant (Dotted);MOShanghai Personage Hygiene Products Co., Ltd.K252622Male Latex Condom HAOkamoto USA, Inc.K252521LifeStyles® HydraFeel Natural Rubber Latex CondomSuretex LimitedK250034Natural rubber latex male condomShaoguan Regenex Pharmaceuticals Co., Ltd.K243421Lelo Hex Lubricated Natural Rubber Latex CondomLelo, Inc.K243640Trojan™ Ultra Ribbed Ecstasy latex condom with lubricant (Trojan™ Ultra Ribbed Ecstasy)Church & Dwight Co., Inc.

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.

↑