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FDA 510(k)

DORC COMPACT MICRO SURGICAL SYSTEM

K-Number: K830216 · 1983-03-09

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

Device Summary

DORC COMPACT MICRO SURGICAL SYSTEM 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 K830216. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORC COMPACT MICRO SURGICAL SYSTEM?

DORC COMPACT MICRO SURGICAL SYSTEM 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 K830216.

When did DORC COMPACT MICRO SURGICAL SYSTEM receive FDA 510(k) clearance?

DORC COMPACT MICRO SURGICAL SYSTEM received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830216.

Who is the listed applicant for DORC COMPACT MICRO SURGICAL SYSTEM?

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 COMPACT MICRO SURGICAL SYSTEM?

The FDA product code for DORC COMPACT MICRO SURGICAL SYSTEM is HQE.

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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

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Related Devices (Code: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development 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.

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