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FDA 510(k)

DORC ADJUSTABLE IMAGE CONTACTS

K-Number: K830169 · 1983-02-07

ApplicantJedmed Instrument Co.
Decision Date1983-02-07
Product CodeHKS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DORC ADJUSTABLE IMAGE CONTACTS 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 1983-02-07 under 510(k) number K830169. The device is classified under product code HKS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORC ADJUSTABLE IMAGE CONTACTS?

DORC ADJUSTABLE IMAGE CONTACTS is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K830169.

When did DORC ADJUSTABLE IMAGE CONTACTS receive FDA 510(k) clearance?

DORC ADJUSTABLE IMAGE CONTACTS received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830169.

Who is the listed applicant for DORC ADJUSTABLE IMAGE CONTACTS?

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 ADJUSTABLE IMAGE CONTACTS?

The FDA product code for DORC ADJUSTABLE IMAGE CONTACTS is HKS.

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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: HKS)

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.

K935302OSHER SURGICAL GONIO/POSTERIOR POLE LENSOcular Instruments, Inc.K895846TWO MIRROR GONIO LENSOcular Instruments, Inc.K890977MCINTYRE SURGICAL GONIOLENSOcular Instruments, Inc.K862692KARICKHOFF DIAGNOSTIC/LASER LENSOcular Instruments, Inc.K862713ABRAHAM IRIDECTOMY LENS (YAG LASER)Ocular Instruments, Inc.K862024SUSSMAN FOUR MIRROR HAND HELD GONIOPRISMOcular Instruments, 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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