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)

HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY

K-Number: K853006 · 1985-09-04

ApplicantModern Diagnostics, Inc.
Decision Date1985-09-04
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY is the device name listed in this FDA 510(k) record. The listed applicant is Modern Diagnostics, Inc.. It received FDA 510(k) clearance on 1985-09-04 under 510(k) number K853006. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY?

HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY is a medical device that received FDA 510(k) clearance on 1985-09-04. The listed applicant is Modern Diagnostics, Inc.. The 510(k) number is K853006.

When did HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY receive FDA 510(k) clearance?

HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY received FDA 510(k) clearance on 1985-09-04, under 510(k) number K853006.

Who is the listed applicant for HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY?

The FDA 510(k) record lists Modern Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY?

The FDA product code for HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCY is JHI.

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

Other records listing Modern Diagnostics, Inc. as applicant

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.

K853269PREGNA/TESTK853258BETA-HCG MICROTITER PREGNANCY TESTK852840ENZYME ANTINUCLEAR ANTIBODY SCREENING TESTK851369ANTINUCLEAR ANTIBODY TEST KIT

Related Devices (Code: JHI)

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.

K262299Instant-View® hCG Combo II Cassette TestAlfa Scientific Designs, Inc.K241919Innovita HCG Pregnancy Rapid Combo TestInnovita (Tangshan) Biological Technology Co., Ltd.K203272Alltest Pregnancy Rapid Combo Test CassetteHangzhou AllTest Biotech Co., Ltd.K172322Atellica IM Total hCG (ThCG)Siemens Healthcare Diagnostics, Inc.K172257TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format)True Diagnostics, Inc.K152768Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test StripAssure Tech. Co., Ltd.

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.

↑