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FDA 510(k)

TYMPANOSCOPE

K-Number: K896274 · 1990-01-26

ApplicantJedmed Instrument Co.
Decision Date1990-01-26
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TYMPANOSCOPE 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 1990-01-26 under 510(k) number K896274. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYMPANOSCOPE?

TYMPANOSCOPE is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K896274.

When did TYMPANOSCOPE receive FDA 510(k) clearance?

TYMPANOSCOPE received FDA 510(k) clearance on 1990-01-26, under 510(k) number K896274.

Who is the listed applicant for TYMPANOSCOPE?

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 TYMPANOSCOPE?

The FDA product code for TYMPANOSCOPE is ERA.

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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: ERA)

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.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, 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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