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FDA 510(k)

DORC CONTACT/PHOTO DERATOSCOPE

K-Number: K830290 · 1983-03-09

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

Device Summary

DORC CONTACT/PHOTO DERATOSCOPE 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 K830290. The device is classified under product code HJA. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORC CONTACT/PHOTO DERATOSCOPE?

DORC CONTACT/PHOTO DERATOSCOPE 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 K830290.

When did DORC CONTACT/PHOTO DERATOSCOPE receive FDA 510(k) clearance?

DORC CONTACT/PHOTO DERATOSCOPE received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830290.

Who is the listed applicant for DORC CONTACT/PHOTO DERATOSCOPE?

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 CONTACT/PHOTO DERATOSCOPE?

The FDA product code for DORC CONTACT/PHOTO DERATOSCOPE is HJA.

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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: HJA)

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.

K901523VKG 1000, VIDEO KERATOGRAPHThe Sanborn Co.K893968VKG 2000 VIDEO KERATOMETERTechnitex, Inc.K842128AMERICAN MEDICAL OPTICS PHOTOKERATOAmerican Medical OpticsK781650TERRY KERATOMETERClifford M. Terry, M.C.

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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