FDA 510(k)

G-N ANAEROBE SUPPLEMENT

K-Number: K822462 · 1982-09-14

Decision Date1982-09-14

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

G-N ANAEROBE SUPPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K822462. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-N ANAEROBE SUPPLEMENT?

G-N ANAEROBE SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K822462.

When did G-N ANAEROBE SUPPLEMENT receive FDA 510(k) clearance?

G-N ANAEROBE SUPPLEMENT received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822462.

Who is the listed applicant for G-N ANAEROBE SUPPLEMENT?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G-N ANAEROBE SUPPLEMENT?

The FDA product code for G-N ANAEROBE SUPPLEMENT is JSK.

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 Oxoid U.S.A., Inc. as applicant

K891593LISTERIA SELECTIVE ENRICHMENT MEDIUM K884026ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KIT K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)K874303STAPHYLASE TEST K872956SORBITOL MACCONKEY AGAR NO. 3 CM 813 K872135MCBRIDE MEDIUM CM 819

View all 93 devices →

Related Devices (Code: JSK)

K881949ATS NAC-PAC SETAlpha-Tec Systems, Inc.K881879ATS M/15 PHOSPHATE BUFFER, PRODUCT #034-42Alpha-Tec Systems, Inc.K881566HEMOGLOBIN POWDERAcumedia Manufacturers, Inc.K861997PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTUREHazleton Research Products, Inc.K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEFlow Laboratories, Inc.K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)Flow Laboratories, 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.