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FDA 510(k)

JEDMED S CHAIR

K-Number: K896298 · 1990-01-26

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

Device Summary

JEDMED S CHAIR 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 K896298. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEDMED S CHAIR?

JEDMED S CHAIR 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 K896298.

When did JEDMED S CHAIR receive FDA 510(k) clearance?

JEDMED S CHAIR received FDA 510(k) clearance on 1990-01-26, under 510(k) number K896298.

Who is the listed applicant for JEDMED S CHAIR?

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 JEDMED S CHAIR?

The FDA product code for JEDMED S CHAIR is ETF.

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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: ETF)

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.

K953457JEDMED SPECTRUM ENT CABINETJedmed Instrument Co.K945395PREMIER MIRROR WARMERPremier Dental Products Co.K932470LANGGASSE 90Happersberger Otopront GmbHK911901MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCEStortzK910781#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCESMidmark Corp.K910243MOBILE TREATMENT CARTJedmed Instrument Co.

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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