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FDA 510(k)

EFFNER FE-EX* OROGASTRIC

K-Number: K874755 · 1988-04-06

Decision Date1988-04-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EFFNER FE-EX* OROGASTRIC is the device name listed in this FDA 510(k) record. The listed applicant is Effner and Spreine Co.. It received FDA 510(k) clearance on 1988-04-06 under 510(k) number K874755. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EFFNER FE-EX* OROGASTRIC?

EFFNER FE-EX* OROGASTRIC is a medical device that received FDA 510(k) clearance on 1988-04-06. The listed applicant is Effner and Spreine Co.. The 510(k) number is K874755.

When did EFFNER FE-EX* OROGASTRIC receive FDA 510(k) clearance?

EFFNER FE-EX* OROGASTRIC received FDA 510(k) clearance on 1988-04-06, under 510(k) number K874755.

Who is the listed applicant for EFFNER FE-EX* OROGASTRIC?

The FDA 510(k) record lists Effner and Spreine Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EFFNER FE-EX* OROGASTRIC?

The FDA product code for EFFNER FE-EX* OROGASTRIC is KNT.

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 Effner and Spreine 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.

Related Devices (Code: KNT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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