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)

CHLAMYDIA & VIRAL TRANSPORT MEDIUM

K-Number: K871065 · 1987-04-14

ApplicantR. Kent Richards, Inc.
Decision Date1987-04-14
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHLAMYDIA & VIRAL TRANSPORT MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is R. Kent Richards, Inc.. It received FDA 510(k) clearance on 1987-04-14 under 510(k) number K871065. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLAMYDIA & VIRAL TRANSPORT MEDIUM?

CHLAMYDIA & VIRAL TRANSPORT MEDIUM is a medical device that received FDA 510(k) clearance on 1987-04-14. The listed applicant is R. Kent Richards, Inc.. The 510(k) number is K871065.

When did CHLAMYDIA & VIRAL TRANSPORT MEDIUM receive FDA 510(k) clearance?

CHLAMYDIA & VIRAL TRANSPORT MEDIUM received FDA 510(k) clearance on 1987-04-14, under 510(k) number K871065.

Who is the listed applicant for CHLAMYDIA & VIRAL TRANSPORT MEDIUM?

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

What is the FDA product code for CHLAMYDIA & VIRAL TRANSPORT MEDIUM?

The FDA product code for CHLAMYDIA & VIRAL TRANSPORT MEDIUM is JSM.

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 R. Kent Richards, 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.

K854452MANNITOL SALT AGARK854450BILE ESCULIN AZIDE AGARK854449HEKTOEN ENTERIC AGARK854454TRYPTIC SOY BLOOD AGARK854457COLUMBIA CNA AGAR W/5% SHEEP BLOODK854455CDC ANAEROBE BLOOD AGAR

View all 12 devices →

Related Devices (Code: JSM)

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.

K242976Medical Wire Fecal Transwab Liquid Cary Blair Medium Collection and Transport DeviceMedical Wire & Equipment Company (Bath), Ltd.K250205Babio® Virus Transport Kit (Non-inactivating)Jinan Babio Biotechnology Co., Ltd.K242576AllTest Viral Transport MediumHangzhou AllTest Biotech Co., Ltd.K232565UriSponge™Copan Italia SpaK220908Ensol EnTM Specimen Collection and Transport SystemEnsol Biosciences, Inc.K240235OmniTrans Transport SystemShenzhen Dakewe Bio-Engineering 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.

↑