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)

DUOFERTILITY

K-Number: K102499 · 2011-12-20

ApplicantCambridge Temperature Concepts , Ltd.
Decision Date2011-12-20
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

DUOFERTILITY is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Temperature Concepts , Ltd.. It received FDA 510(k) clearance on 2011-12-20 under 510(k) number K102499. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOFERTILITY?

DUOFERTILITY is a medical device that received FDA 510(k) clearance on 2011-12-20. The listed applicant is Cambridge Temperature Concepts , Ltd.. The 510(k) number is K102499.

When did DUOFERTILITY receive FDA 510(k) clearance?

DUOFERTILITY received FDA 510(k) clearance on 2011-12-20, under 510(k) number K102499.

Who is the listed applicant for DUOFERTILITY?

The FDA 510(k) record lists Cambridge Temperature Concepts , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUOFERTILITY?

The FDA product code for DUOFERTILITY is LHD.

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: LHD)

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.

K200163Ava Fertility TrackerAva AGK122337OVUSENSEFertility Focus, Ltd.K050094LADY COMP USALady Comp USAK030961MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921Microlife Corp.K021978PETIT SOPHIANishitomo Co., Inc.K002726TCOYF FERTILITY SOFTWARE VERSION 1.0Ovusoft, LLC

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.

↑