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FDA 510(k)

KANAMYCIN RIA

K-Number: K772038 · 1978-01-12

ApplicantMonitor Science Corp.
Decision Date1978-01-12
Product CodeKJI
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

KANAMYCIN RIA is the device name listed in this FDA 510(k) record. The listed applicant is Monitor Science Corp.. It received FDA 510(k) clearance on 1978-01-12 under 510(k) number K772038. The device is classified under product code KJI. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KANAMYCIN RIA?

KANAMYCIN RIA is a medical device that received FDA 510(k) clearance on 1978-01-12. The listed applicant is Monitor Science Corp.. The 510(k) number is K772038.

When did KANAMYCIN RIA receive FDA 510(k) clearance?

KANAMYCIN RIA received FDA 510(k) clearance on 1978-01-12, under 510(k) number K772038.

Who is the listed applicant for KANAMYCIN RIA?

The FDA 510(k) record lists Monitor Science Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KANAMYCIN RIA?

The FDA product code for KANAMYCIN RIA is KJI.

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 Monitor Science Corp. 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.

K790580RIA KIT, PROSTATIC ACIDK780949BIO-MONITOR AMIKACINK780950BIO-MONITOR TOBRAMYCINK780951BIO-MONITOR GENTAMICINK772039BETA-HCG RIA

Related Devices (Code: KJI)

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.

K832769AMES TDA KANAMYCIN TEST-CONTROL SERUMMiles Laboratories, Inc.K823370ADVANCE TM EMIT(R) & TM AMIKACIN ASSAYSyva Co.K823062KENAMYCIN FLUORESCENT IMMUNOASSAY FIAAmerican Diagnostic Corp.K822808TDX KENAMYCINAbbott LaboratoriesK782125RIA KIT, KANAMYCINDiagnostic Products Corp.

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.

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