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FDA 510(k)

ATMOS ENT PATIENT CHAIR #1

K-Number: K791937 · 1979-11-13

ApplicantJedmed Instrument Co.
Decision Date1979-11-13
Product CodeETL
DecisionSubstantially Equivalent

Device Summary

ATMOS ENT PATIENT CHAIR #1 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 1979-11-13 under 510(k) number K791937. The device is classified under product code ETL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATMOS ENT PATIENT CHAIR #1?

ATMOS ENT PATIENT CHAIR #1 is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K791937.

When did ATMOS ENT PATIENT CHAIR #1 receive FDA 510(k) clearance?

ATMOS ENT PATIENT CHAIR #1 received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791937.

Who is the listed applicant for ATMOS ENT PATIENT CHAIR #1?

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 ATMOS ENT PATIENT CHAIR #1?

The FDA product code for ATMOS ENT PATIENT CHAIR #1 is ETL.

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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: ETL)

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.

K791938ATMOS ENT PATIENT CHAIR #5Jedmed Instrument Co.K781218ANEMOMETER, NASAL, EXETERMedika Corp.K772193NASSAL PRESSURE/FLOW RECORDERAdco Labs.

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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