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)

MINIATURE ION SELECTIVE ELECTRODES

K-Number: K830130 · 1983-03-07

ApplicantIonetics, Inc.
Decision Date1983-03-07
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINIATURE ION SELECTIVE ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Ionetics, Inc.. It received FDA 510(k) clearance on 1983-03-07 under 510(k) number K830130. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIATURE ION SELECTIVE ELECTRODES?

MINIATURE ION SELECTIVE ELECTRODES is a medical device that received FDA 510(k) clearance on 1983-03-07. The listed applicant is Ionetics, Inc.. The 510(k) number is K830130.

When did MINIATURE ION SELECTIVE ELECTRODES receive FDA 510(k) clearance?

MINIATURE ION SELECTIVE ELECTRODES received FDA 510(k) clearance on 1983-03-07, under 510(k) number K830130.

Who is the listed applicant for MINIATURE ION SELECTIVE ELECTRODES?

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

What is the FDA product code for MINIATURE ION SELECTIVE ELECTRODES?

The FDA product code for MINIATURE ION SELECTIVE ELECTRODES is JSG.

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 Ionetics, 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.

K932179MODEL 400/450 ELECTROLYTE ANALYZERK895397CALCIUM AND PH ELECTROLYTE ANALYZERK890792POTASSIUM AND SODIUM ELECTROLYTE ANALYZERK863907MODIFIED SODIUM ELECTRODEK851808ELECTROLYTE ANALYZERK802856MINIATURE ION SELECTIVE ELECTRODES

View all 7 devices →

Related Devices (Code: JSG)

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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia Manufacturers, 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.

↑