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FDA 510(k)

JEDMED MAXIM ENT CABINET

K-Number: K881958 · 1988-07-15

Decision Date1988-07-15
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

JEDMED MAXIM ENT CABINET 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 1988-07-15 under 510(k) number K881958. 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 MAXIM ENT CABINET?

JEDMED MAXIM ENT CABINET is a medical device that received FDA 510(k) clearance on 1988-07-15. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K881958.

When did JEDMED MAXIM ENT CABINET receive FDA 510(k) clearance?

JEDMED MAXIM ENT CABINET received FDA 510(k) clearance on 1988-07-15, under 510(k) number K881958.

Who is the listed applicant for JEDMED MAXIM ENT CABINET?

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 MAXIM ENT CABINET?

The FDA product code for JEDMED MAXIM ENT CABINET is ETF.

Related Clinical Trials

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.

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.

View all 91 devices →

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.

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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