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FDA 510(k)

OPHTEC RUST RING REMOVER

K-Number: K834354 · 1984-03-19

ApplicantJedmed Instrument Co.
Decision Date1984-03-19
Product CodeHOG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTEC RUST RING REMOVER 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 1984-03-19 under 510(k) number K834354. The device is classified under product code HOG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTEC RUST RING REMOVER?

OPHTEC RUST RING REMOVER is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K834354.

When did OPHTEC RUST RING REMOVER receive FDA 510(k) clearance?

OPHTEC RUST RING REMOVER received FDA 510(k) clearance on 1984-03-19, under 510(k) number K834354.

Who is the listed applicant for OPHTEC RUST RING REMOVER?

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 OPHTEC RUST RING REMOVER?

The FDA product code for OPHTEC RUST RING REMOVER is HOG.

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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: HOG)

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.

K962989AMOILS EPITHELIAL SCRUBBERS. Percy AmoilsK960261PALLIKARIS BRUSHAlcon Laboratories, Inc.K950520BURR, CORNEAL, BATTERY-POWEREDAaron Medical IndustriesK883785GY-RO SAFEGy-Ro Industry, 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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