FDA 510(k)

ISOLATION OF PATHOGENIC NEISSERIA

K-Number: K820847 · 1982-04-16

Decision Date1982-04-16

Product CodeJTY

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ISOLATION OF PATHOGENIC NEISSERIA is the device name listed in this FDA 510(k) record. The listed applicant is Blue Ridge Media Co.. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K820847. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOLATION OF PATHOGENIC NEISSERIA?

ISOLATION OF PATHOGENIC NEISSERIA is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Blue Ridge Media Co.. The 510(k) number is K820847.

When did ISOLATION OF PATHOGENIC NEISSERIA receive FDA 510(k) clearance?

ISOLATION OF PATHOGENIC NEISSERIA received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820847.

Who is the listed applicant for ISOLATION OF PATHOGENIC NEISSERIA?

The FDA 510(k) record lists Blue Ridge Media Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ISOLATION OF PATHOGENIC NEISSERIA?

The FDA product code for ISOLATION OF PATHOGENIC NEISSERIA is JTY.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Blue Ridge Media Co. as applicant

K820848BLUE RIDGE SHEEP BLOOD K820840CULTURE MEDIA, GENERAL NUTRIENT BROTH K820845DULTURE MEDIA, SELECTIVE & NON-DIFFER K820842CULTURE MEDIA, NON-SELECTIVE/DIFFER K820844CULTURE MEDIA, SELECTIVE & DIFFERENTIAL K820843CULTURE MEDIA SELECTIVE BROTH

View all 11 devices →

Related Devices (Code: JTY)

K210511InTray GCBiomed Diagnostics Incorporated K993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, 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.