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)

DORC INTRAOCULAR ELECTROMAGNET

K-Number: K830336 · 1983-03-09

ApplicantJedmed Instrument Co.
Decision Date1983-03-09
Product CodeHPO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DORC INTRAOCULAR ELECTROMAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830336. The device is classified under product code HPO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORC INTRAOCULAR ELECTROMAGNET?

DORC INTRAOCULAR ELECTROMAGNET is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K830336.

When did DORC INTRAOCULAR ELECTROMAGNET receive FDA 510(k) clearance?

DORC INTRAOCULAR ELECTROMAGNET received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830336.

Who is the listed applicant for DORC INTRAOCULAR ELECTROMAGNET?

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

What is the FDA product code for DORC INTRAOCULAR ELECTROMAGNET?

The FDA product code for DORC INTRAOCULAR ELECTROMAGNET is HPO.

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 Jedmed Instrument Co. 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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K953457JEDMED SPECTRUM ENT CABINETK950925JEDMED LARYNGEAL SCOPEK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

View all 91 devices →

Related Devices (Code: HPO)

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.

K854870INTRAOCULAR ELECTROMAGNETMira, Inc.K832950SCIENTRONICS 10K EYE MAGNETScientific Manufacturer

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.

↑