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FDA 510(k)

LID CHAIN EYELID WEIGHTS

K-Number: K021750 · 2003-01-27

ApplicantJedmed Instrument Co.
Decision Date2003-01-27
Product CodeMML
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LID CHAIN EYELID WEIGHTS 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 2003-01-27 under 510(k) number K021750. The device is classified under product code MML. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LID CHAIN EYELID WEIGHTS?

LID CHAIN EYELID WEIGHTS is a medical device that received FDA 510(k) clearance on 2003-01-27. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K021750.

When did LID CHAIN EYELID WEIGHTS receive FDA 510(k) clearance?

LID CHAIN EYELID WEIGHTS received FDA 510(k) clearance on 2003-01-27, under 510(k) number K021750.

Who is the listed applicant for LID CHAIN EYELID WEIGHTS?

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 LID CHAIN EYELID WEIGHTS?

The FDA product code for LID CHAIN EYELID WEIGHTS is MML.

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Other records listing Jedmed Instrument Co. as applicant

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K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K950925JEDMED LARYNGEAL SCOPEK953457JEDMED SPECTRUM ENT CABINETK950785HORTMANN AIRMATIC AIR CALORIC STIMULATORK950078MICROFLOW IRRIGATION SYSTEM

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Related Devices (Code: MML)

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.

K170591Altomed Malhotra Platinum SegmentsAltomed LimitedK011740CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)Meddev Corp.K011115KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010Heinz Kurz GmbH MedizintechnikK003646SUTUREGROOVE WEIGHT SIZING SETIop, Inc.K001123KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111Heinz Kurz GmbH MedizintechnikK994289SUTUREGROOVEIop, 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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