EFFNER FE-EX* OROGASTRIC
K-Number: K874755 · 1988-04-06
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.