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)

AFRICAN GREEN SV 5/SV 40

K-Number: K843252 · 1984-09-06

ApplicantViromed Laboratories, Inc.
Decision Date1984-09-06
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AFRICAN GREEN SV 5/SV 40 is the device name listed in this FDA 510(k) record. The listed applicant is Viromed Laboratories, Inc.. It received FDA 510(k) clearance on 1984-09-06 under 510(k) number K843252. The device is classified under product code KIR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFRICAN GREEN SV 5/SV 40?

AFRICAN GREEN SV 5/SV 40 is a medical device that received FDA 510(k) clearance on 1984-09-06. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K843252.

When did AFRICAN GREEN SV 5/SV 40 receive FDA 510(k) clearance?

AFRICAN GREEN SV 5/SV 40 received FDA 510(k) clearance on 1984-09-06, under 510(k) number K843252.

Who is the listed applicant for AFRICAN GREEN SV 5/SV 40?

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

What is the FDA product code for AFRICAN GREEN SV 5/SV 40?

The FDA product code for AFRICAN GREEN SV 5/SV 40 is KIR.

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 Viromed Laboratories, 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.

K951440LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTUREK951461NCI-H292 CELL CULTUREK871613BUFFALO GREEN MONKEY KIDNEY CELLSK862555HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA)K861373HUMAN LUNG CARCINOMA CELLS (A549)K853695RESPIRATORY SYNCYTIAL VIRUS ID REAGENT

View all 25 devices →

Related Devices (Code: KIR)

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.

K973212FRESH CELLS WI-38Diagnostic Hybrids, Inc.K973210FRESH CELLS NCI H292Diagnostic Hybrids, Inc.K973209FRESH CELLS VERODiagnostic Hybrids, Inc.K973211FRESH CELLS MV1LUDiagnostic Hybrids, Inc.K973213FRESH CELLS LLC-MK2Diagnostic Hybrids, Inc.K973214FRESH CELLS HFFDiagnostic Hybrids, 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.

↑