EVOPORT 100
K-Number: K863985 · 1987-01-29
Advertisement
Device Summary
Frequently Asked Questions
What is the EVOPORT 100?
EVOPORT 100 is a medical device that received FDA 510(k) clearance on 1987-01-29. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K863985.
When did EVOPORT 100 receive FDA 510(k) clearance?
EVOPORT 100 received FDA 510(k) clearance on 1987-01-29, under 510(k) number K863985.
Who is the listed applicant for EVOPORT 100?
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 EVOPORT 100?
The FDA product code for EVOPORT 100 is GWJ.
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.
Related Devices (Code: GWJ)
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.
Advertisement